ID HSA_10148_EBI3 standard; DNA; HUM; 1100 BP. XX AC 10148; XX DT 06-Sep-2005 (Created) XX DE EBI3: Epstein-Barr virus induced gene 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.19 4179508..4180607 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 19p13.3 XX CC Database Reference HGNC: 3129; EBI3 CC Database Reference ENTREZGENE: 10148 CC Database Reference UNIGENE: Hs.501452 CC Database Reference ENSEMBL: ENSG00000105246 CC Database Reference REFSEQ: NM_005755 CC Database Reference REFSEQ: NP_005746 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219424_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219424_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219424_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="19" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 4179508..4180607" FT /note="Genomic Strand: FORWARD" FT prim_transcript 988..>988 FT /db_xref="ENSEMBL:ENST00000221847" FT prim_transcript 1013..>1013 FT /db_xref="dbTSS:PLR00644" XX SQ Sequence 1100 BP; 89 A; 431 C; 201 G; 379 T; 0 other; tctgtctctg tctctgtcat ctccctgtct atctccgtgt cctcctcctc tcatctctgc 60 ctttctcatc tctgtgtctc tctctgtgtt tctgtctctg tcatgcccct ttctctgtct 120 gtcatctccc tgtctctatc tatctctgtg tcctcctcct ctcatctctg tctctctcat 180 ctgtatctct ctctgtctct gtcgtctccc tgtctctcta tctctttgtc ctcttcctct 240 tgtctttctc tctgcctctc tcatctgtgt ctctctctgt ctctgtctct gtcatctccc 300 tgtctctgtc tctctctctc tgtgtcctcc tcctctcgtc tctttctctc tgcctctttc 360 atctgtgtct ctgtgtctct ctgtcatctc cctgtctatc tctgtgtcct cctcctctcg 420 tctctgtctc tctgcctctt tcatctgtgt ctctctgtct ctgtctctgt catctccctg 480 tctctgtatc cctctatctc tgtgtcctcc tcttcttgtc tctgtctctc tgcctctctc 540 atctgtgtct ctctctgtgt ctctgtctct gtcatctccc tgtctctctg tgtcttcctt 600 ctgtcttctc tgtctctctg cctctctccc ccatctctgc ctctgtctcc ctccatgtcc 660 ctgagcccct gcctgcctgc ctggggtttc ccccgcttca gggcagcgga aggaaggcca 720 gcaggacatg ctgtgctggg aaaagccagc aggtctccac ttctcccttt cacagcctcc 780 tcccccgccc ccaccctcgg ggccttccga gcaggggtgg cctgtgctcc ccagggggct 840 ggggctcctc cacaccctaa ttcatctccc tagcggcccc acgagcccca ccagtgagtc 900 agacctgaag gaagtcgggg agggggcggg ccttgaccct gggctgggct ttcccctggg 960 caggtcccaa gtcctcacct cccctctcaa gtctcccacg acgttcccac ccactcctga 1020 gagcagagct ggccgcagcc atgaccccgc agcttctcct ggcccttgtc ctctgggcca 1080 gctgcccgcc ctgcagtgga 1100 // ID HSA_10318_1_TNIP1 standard; DNA; HUM; 1100 BP. XX AC 10318_1; XX DT 07-Sep-2005 (Created) XX DE TNIP1: TNFAIP3 interacting protein 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 150440659..150441758 (REVERSE) CC Score Points: 13 (61.9%) CC Chromosomal Location: 5q32-q33.1 XX CC Database Reference HGNC: 16903; TNIP1 CC Database Reference ENTREZGENE: 10318 CC Database Reference UNIGENE: Hs.355141 CC Database Reference ENSEMBL: ENSG00000145901 CC Database Reference REFSEQ: NM_006058 CC Database Reference REFSEQ: NP_006049 CC Database Reference AFFYMETRIX: AFFY_HG_U95D:82059_i_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207196_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38970_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38971_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207196_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:82061_r_at CC Database Reference TRANSFAC GENE: G006830; TNIP1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 150440659..150441758" FT /note="Genomic Strand: REVERSE" FT prim_transcript 915..>915 FT /db_xref="ENSEMBL:ENST00000315050" FT prim_transcript 931..>931 FT /db_xref="dbTSS:HRC07480" FT prim_transcript 972..>972 FT /db_xref="dbTSS:KMR01669" FT prim_transcript 982..>982 FT /db_xref="dbTSS:KGR02355" FT /note="Number of reported TSSs: 2" FT prim_transcript 998..>998 FT /db_xref="dbTSS:MPG01564" FT prim_transcript 1018..>1018 FT /db_xref="dbTSS:KAR01648" FT prim_transcript 1021..>1021 FT /db_xref="dbTSS:HSI01942" FT /note="Number of reported TSSs: 3" FT prim_transcript 1022..>1022 FT /db_xref="dbTSS:CAS07044" FT prim_transcript 1052..>1052 FT /db_xref="dbTSS:TIR08219" FT prim_transcript 1070..>1070 FT /db_xref="dbTSS:KGR01617" XX SQ Sequence 1100 BP; 214 A; 302 C; 322 G; 262 T; 0 other; ggtttttcat aaagctatat ttagtttaaa gagctgttct ttattccaag gttagacctt 60 ccactttttg gaattaaaat ttagctttct ttctttttaa aaataaaagg ataagctttt 120 aaaaagcttt cctaccctta aagcaagttt atgttcctta ccggtctagg aaatcccagt 180 ctgttgggat tatctagccc acatataagt aggtagggtg gaaggcggcc tctggatttg 240 cccacccggg tttgaatctt gattcagccc cttactgagg tcatctaacc tttttgtgac 300 tcaaatatta tttaagaaaa ggtagtaaaa cccacctccc tagcgtgatt gtgcgaagaa 360 aataatgcac gcaaagcatc tacaatgtct ggagcaaagc gtttacgatg tctgggaatc 420 ctttacaatg tctggagcaa aaaatgttcg cggtagagtc tttatgggtc ttttcagctc 480 ggaatttcta tagctttgtt aagaagagtc ctggagtgcc ctggacggaa ctctgggggc 540 ctgagctcca gctctggctt agggccaaat gcttacgtgc cttttggcag gtcccctccc 600 tgttctggcc tgtgttcccc tcggcacaag gaaggggctg ggtggtctct gtggctcgcc 660 tccgctctga aattccggct ttcaaggtgg ccccaggcct tcgacagggg cttccggcgc 720 tgggagtgcg gcaaggcgcc gcgcaggccc gggacggtgg ccccagggaa gtcgctccta 780 gaggggaagg ccgccgaagg gacgagagac accgcgggcc cccggaaccg caggcagccg 840 gtgtttacct cgctcggtcc caccccaggc ggccgcgggc ccgcccggag cgcgcggcgc 900 gattgggcga gtggcctgcc agtctccggg gactttccca ggggtggggc ggcccggcca 960 ggcccccggc acttcctcgt cctcggcccg ggtgccctgc ccccgtccag gagccctagg 1020 agtgctacgg ggggccggag ccttgcccgg gccgctgccc cgtccctgga ttcggggctg 1080 gacgcagcaa gcggggcgct 1100 // ID HSA_10384_BTN3A3 standard; DNA; HUM; 1100 BP. XX AC 10384; XX DT 06-Sep-2005 (Created) XX DE BTN3A3: butyrophilin, subfamily 3, member A3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 26547743..26548842 (FORWARD) CC Score Points: 4 (57.1%) CC Chromosomal Location: 6p21.3 XX CC Database Reference HGNC: 1140; BTN3A3 CC Database Reference ENTREZGENE: 10384 CC Database Reference ENSEMBL: ENSG00000111801 CC Database Reference REFSEQ: NM_006994 CC Database Reference REFSEQ: NM_197974 CC Database Reference REFSEQ: NP_932078 CC Database Reference REFSEQ: NP_008925 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:38241_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204821_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204821_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204820_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204821_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204820_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:38241_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204820_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38241_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:38241_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 26547743..26548842" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1000..>1000 FT /db_xref="ENSEMBL:ENST00000244519" FT /note="Number of reported TSSs: 3" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:SYN01475" XX SQ Sequence 1100 BP; 368 A; 233 C; 187 G; 312 T; 0 other; ctggtatcta tgagatagca gagcctattg aagtacccaa gaaaattagg ctttatcacc 60 aagaagaaag ggggactgca tgatgcagaa gggaccagcc atctcaacca gatactgcac 120 agcctaaatt caaactgtta caatataatc aaatttcatc aaccccagtc acatcttaat 180 cttaggagtt ttgatcactg acttgcaaat ccaaaaagtg tgttttgagg tcctaggcca 240 caggaagaac cagtttgtct cacagacctc ttacagagat ggcatttgta gtctatctag 300 attccagctt cagataatat gtactccact ggcagcacga gaaataaata cacaggaaaa 360 tacaatatag cacaaaccag gagctgaggg cgaatgaaga tgctcagaaa cacctgcact 420 aaaagtttcc tgaaaaaggt aaaaaatgtc aatcagcact gcctctggaa accagaaaca 480 ttatattatt tgataacaga tcctaagtct ggatgctgga ggtgcttaaa aatgtgcatt 540 gcgtctggct ttctttccat gtatacattt atttgacgct gtagtaaaat ctcctccttc 600 aggtacccat attcatgcaa gcaaatgtta gcaaactgcc acagtagcat tttaattagt 660 gcacaacttt ctctcttcac cacattataa tcttttctca ttttgttctg ctgctatttc 720 tattatgata aaagacttaa gtaaatatgt agaaatactt atatacatgg acacgcaata 780 atgattcaaa tagataaaca cagaaacaca aacactaagg gaggtacggc tggaattttt 840 ctgcaacgtg tacaattcaa tgtactttca cttttcattt caaccctcct cagtggtttc 900 ctcccagcaa ctgatgagaa acatcacctc tgagccaatc aaaaaactaa ttcttccaaa 960 aagagattgt tattattcct cacaataacc agatagcctc tgctttcttt ttcctttctt 1020 cggaatgaga gactcaacca taatagaaag aatggagaac tattaaccac cattcttcag 1080 tgggctgtga ttttcagagg 1100 // ID HSA_11182_SLC2A6 standard; DNA; HUM; 1100 BP. XX AC 11182; XX DT 06-Sep-2005 (Created) XX DE SLC2A6: solute carrier family 2 (facilitated glucose transporter), DE member 6 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.9 133373673..133374772 (REVERSE) CC Score Points: 11 (78.6%) CC Chromosomal Location: 9q34 XX CC Database Reference HGNC: 11011; SLC2A6 CC Database Reference ENTREZGENE: 11182 CC Database Reference UNIGENE: Hs.244378 CC Database Reference ENSEMBL: ENSG00000160326 CC Database Reference REFSEQ: NM_017585 CC Database Reference REFSEQ: NP_060055 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:220091_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:220091_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:220091_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:75122_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="9" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 133373673..133374772" FT /note="Genomic Strand: REVERSE" FT prim_transcript 961..>961 FT /db_xref="dbTSS:LFL08521" FT prim_transcript 993..>993 FT /db_xref="dbTSS:T7R03404" FT prim_transcript 997..>997 FT /db_xref="dbTSS:LFL09233" FT /note="Number of reported TSSs: 2" FT prim_transcript 998..>998 FT /db_xref="dbTSS:LFL04012" FT /note="Number of reported TSSs: 4" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000291725" FT /db_xref="dbTSS:CAS10916" FT prim_transcript 1074..>1074 FT /db_xref="dbTSS:JTH02685" XX SQ Sequence 1100 BP; 211 A; 339 C; 340 G; 210 T; 0 other; aaaataggca catgaggaaa agactggaag aggctaaaac gccatcaagg tcaggctgac 60 gggagatgga tgtgatttta ttgttctatt atggttgtat ttcaatcata ataaaaggga 120 attctaactt ttaaaaatgc tttaccatgt taatagctaa aatgggaaat gacccaaata 180 ctcagcaaca aaggctccgt ttaaaagcgt gtgtggcacg tccatccaac agagcagggc 240 gtgattccgt cctcttcccg aaaaggccca aagggagagg tggaactgct gtgggatttt 300 ttgaggacgg tcttcccggg aattttccat ttctgctttt cttatttttc aatgttatct 360 tactacctgg gttacgtgtc acgagctcag gttatttcta ccaccagagc ctggggtgga 420 ggatacagac ctcgcccact ggagctgccc acagcgcctc gccggcccct cctgcctcct 480 tcgtcccgca catccgctgc tgccctgaca caccccgatt ccctggtgcc agggagagcc 540 agggcagagg tggccctgag acgccacgcg acggggaggg ctagagcgta aggaggagcg 600 aggtgcgcat tcgctgtgac cctggcgctc ggcttcgcct ctctgggcct cggtttccac 660 cccgcgggag cgagtacgac aggggctgcg cgcattgccg cagtcacgcc tgcaagagcc 720 gggccgggtg agccgcttcc ggcgctccgc gggggccccg gacgatccag caggggctcc 780 gccctgggac ccccatcctg tcttggggcg tgaccttcgg gggcgcacgc ggtgccggcc 840 gcgcccgggg aagccgggtc cgcatccgag catcaggaca gcctgcggcc gccccattgg 900 ccggcgtgtc tctgcagggc cgtcccacag ccaatagcgg ccaaggggcg gagcctggcc 960 ggtgccctcg gagctgctgg ccccgggcgg ctgctccagt ctgagcgccc tccgctcgcc 1020 ccgagagaga cccggccatg caggagccgc tgctgggagc cgagggcccg gactacgaca 1080 ccttccccga gaagccgccc 1100 // ID HSA_127544_IBRDC3 standard; DNA; HUM; 1100 BP. XX AC 127544; XX DT 08-Sep-2005 (Created) XX DE IBRDC3: IBR domain containing 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 33099344..33100443 (REVERSE) CC Score Points: 2 (66.7%) CC Chromosomal Location: 1p35.1 XX CC Database Reference HGNC: 26886; IBRDC3 CC Database Reference ENTREZGENE: 127544 CC Database Reference UNIGENE: Hs.546478 CC Database Reference ENSEMBL: ENSG00000116514 CC Database Reference REFSEQ: NP_699172 CC Database Reference REFSEQ: NM_153341 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36564_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:36564_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:36564_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213038_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:36564_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213038_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213038_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 33099344..33100443" FT /note="Genomic Strand: REVERSE" FT prim_transcript 937..>937 FT /db_xref="ENSEMBL:ENST00000356990" FT prim_transcript 1065..>1065 FT /db_xref="ENSEMBL:ENST00000235150" XX SQ Sequence 1100 BP; 267 A; 267 C; 314 G; 252 T; 0 other; tcagtgagct gtgatcacgc cactgcactc caacctgggt gacagagcaa aaccgtctca 60 ggaaaaaaaa taaataaatt tcaatcgtaa gctatttttt tcttttgtta tttgcaattg 120 aatgtaatcc tgatacattc ctgttgttga agctgtttgc ctgcctccca ctaggaagcc 180 taagggtcca gatcctcccc cagtcagagg aatggggaac tagaaaaaga aaggcaaagg 240 cactgccagg caagaaaacg ctgggtctcc ttccacaagt ttggtaagta agcaagatac 300 caggaggata gaatggtaag tgagcctaga aatagactat tatatacata gggtttatta 360 aatacataga gaacactgaa tgctagacta agaaatttgg actttattct ggaagtccct 420 tgcaataggg gaccttgtct gttttatttt ctaatgcctc gcactttgta gaagctcagt 480 gaatgaatat attctttatt aatttatgcc gtctgcttaa taaacagaaa tgttggaagg 540 tgaaccagtt gggagtcacc atctgatcaa cccctgcctg ctttttataa ataatgtaac 600 tgaaccatca tttactggaa gtggcaatca acctgtgagg aacggcaaac caaaaagtcc 660 accttgggtg tcatggtgat ggaattggag gcggagacca gggagagcag cgggctagga 720 tctctgagag tctccgcaac atggcggccc tggaaccacc tgaccggcag gaggcggagc 780 tccgccccag ctcgctcggc cccaccccgc tcggccctgc ccagcgcact cctagaccgg 840 ggcgcaaggg ttgtgaggtg tttgagcgaa gcgcctgcgc agggcagcgg cgcgcggggc 900 ggaggcttta taatcacttc gtcgttgccg ctcggcttct atcgccggga gggcggttga 960 ggcggtggtg gcggcgtcgg cggcggccgg gcgctggctg aggggcgctg aggcgggagc 1020 tgtggcggcg ctgggcgccc ctggctcctc ggcctctgcc ggccatgggc tccgagaagg 1080 actccgagtc gccgcgctcc 1100 // ID HSA_1318_SLC31A2 standard; DNA; HUM; 1100 BP. XX AC 1318; XX DT 06-Sep-2005 (Created) XX DE SLC31A2: solute carrier family 31 (copper transporters), member 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.9 112991840..112992939 (FORWARD) CC Score Points: 75 (97.4%) CC Chromosomal Location: 9q31-q32 XX CC Database Reference HGNC: 11017; SLC31A2 CC Database Reference ENTREZGENE: 1318 CC Database Reference UNIGENE: Hs.24030 CC Database Reference ENSEMBL: ENSG00000136867 CC Database Reference REFSEQ: NM_001860 CC Database Reference REFSEQ: NP_001851 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204204_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204204_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34749_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204204_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="9" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 112991840..112992939" FT /note="Genomic Strand: FORWARD" FT prim_transcript 937..>937 FT /db_xref="dbTSS:HRT00129" FT prim_transcript 953..>953 FT /db_xref="dbTSS:STM01870" FT misc_feature 964 FT /note="SECONDARY ANCHOR: MMU [20530]; Alignment" FT prim_transcript 966..>966 FT /db_xref="dbTSS:SLV06540" FT prim_transcript 971..>971 FT /db_xref="dbTSS:MPB05917" FT /note="Number of reported TSSs: 5" FT prim_transcript 975..>975 FT /db_xref="dbTSS:RCT04441" FT /note="Number of reported TSSs: 3" FT prim_transcript 995..>995 FT /db_xref="dbTSS:SLV05809" FT prim_transcript 996..>996 FT /db_xref="dbTSS:SLV09339" FT prim_transcript 999..>999 FT /db_xref="dbTSS:CCR01190" FT /note="Number of reported TSSs: 2" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [20530]; Alignment" FT prim_transcript 1002..>1002 FT /db_xref="ENSEMBL:ENST00000259392" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:MPE01533" FT prim_transcript 1007..>1007 FT /db_xref="EPD:EP73235" FT misc_feature 1007 FT /note="PRIMARY ANCHOR: MMU [20530]; Alignment" FT prim_transcript 1035..>1035 FT /db_xref="dbTSS:MPB07305" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 316 A; 263 C; 269 G; 252 T; 0 other; agcctgggcg acagagcgag actctgtttc aaagaaaaga aaaaaagctg tgtgaccctg 60 aggattctac catttactga acaagctccc actgccaggt tacatgataa tttaacatgt 120 atgttttcat ttaatcccta tgacatagat tttattatta ttttcatttt actgaccaga 180 aaactgaggt tcagagatgt aagctatttg cctacggtcc caaagccaat agttgatgcg 240 tatggatgtg aactgaggtt agctccaggc tcaaggtctc tgctaatact gtccttagta 300 aggtttctct gaagagcctc tttactcata ggctgattag caaagggttc ctaaatatgc 360 ttaagaatca ataaccatta aaaatccctc accctacaag aaactcccca tcaaaaaact 420 ggatcagtga aatgaacagg caatacacag aaatggaagt acccgtaaga aaaatagttt 480 actaccctag taatcaaaga aaaacaaaat tacacgggtg tattcctttt ggcttatcag 540 attggaaaat atttttctaa aaagaaaaat gtaattatct tgtaatgact acactaaaaa 600 tctagggcat aattgactta atttactcca aatgtgttgc tattgcgtcc atagcacgga 660 cttgcccatt tcaactcaat atatgttacg cttggggtag tttattacaa tgagcaataa 720 acattctcat aatcgccaag acaagccaag tgcaaaacag gaagggcgaa gacagagggc 780 agcaggtggt ccctctcgct cgcgactccg ggaacgccaa gcctcagccc ttgggaacct 840 ggggcgaggc gcctgggtct cggccagggg gcgcgcccga ggacgccgaa gtagggcgcg 900 tgtggggacc acaactccca ggcgcccgcg cgccgcctcg cccggaccac gtgatccgtg 960 cggccagggt agctatcgcg gcggcggcgg cggcggcggt tgaactgact cggagcgagg 1020 agacccgagc gagcagacgc ggccctggcg cccgccctgc gcactcacca tggcggtaag 1080 ggccgggcgc tacggtgaag 1100 // ID HSA_1435_CSF1 standard; DNA; HUM; 1100 BP. XX AC 1435; XX DT 06-Sep-2005 (Created) XX DE CSF1: colony stimulating factor 1 (macrophage) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 110164509..110165608 (FORWARD) CC Score Points: 53 (100.0%) CC Chromosomal Location: 1p21-p13 XX CC Database Reference HGNC: 2432; CSF1 CC Database Reference ENTREZGENE: 1435 CC Database Reference UNIGENE: Hs.173894 CC Database Reference ENSEMBL: ENSG00000184371 CC Database Reference REFSEQ: NP_000748 CC Database Reference REFSEQ: NP_757351 CC Database Reference REFSEQ: NM_172211 CC Database Reference REFSEQ: NM_172212 CC Database Reference REFSEQ: NM_172210 CC Database Reference REFSEQ: NP_757349 CC Database Reference REFSEQ: NP_757350 CC Database Reference REFSEQ: NM_000757 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211839_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209716_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210557_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210557_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207082_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207082_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207082_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:882_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209716_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211839_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211839_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210557_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209716_at CC Database Reference TRANSFAC GENE: G005956; CSF1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 110164509..110165608" FT /note="Genomic Strand: FORWARD" FT prim_transcript 991..>991 FT /db_xref="ENSEMBL:ENST00000329608" FT /note="Number of reported TSSs: 3" FT prim_transcript 1002..>1002 FT /db_xref="EPD:EP37006" FT misc_feature 1002 FT /note="SECONDARY ANCHOR: MMU [12977]; Alignment" XX SQ Sequence 1100 BP; 231 A; 274 C; 366 G; 229 T; 0 other; cccagggggt ggaaacgggc aacctcacag aggaattgaa tcataatgaa ttgaagaaag 60 aaaaatctcc tgaagttggc attataatta ataggcttag gctcatccta ctagtcctca 120 cttagactca ttctcatgta gaaacaaaac gtgattaatc acctcagtaa gtgcaatttc 180 caaaaacatc cagggaaatc tagggtccag gtgcaggacc tttccaatct gagttggatt 240 ttgcctccag gagagagcat gggtaccagc cagcattttc atcatctaag ggtcaggtgc 300 cttgaagtgt ctgctggcac ccagggaaga gccccccagc ttgctgtcac aggacacagc 360 tgctcccttc ctggccaggt agctggcctc cctcccagaa tgggacttga agctggccgg 420 gctgcttggg ggctgcagag gaagaagggg gctgccggca aacctgctga ctcaggctcc 480 acgagggagc aagtaacact ggactccttt cggcactccg agaatggggt gggggcgtct 540 tcaaaggatt tccctccctt cccagtgctt gtccctgctc tcggtccgtt ttctgctaag 600 atttggggat tttcaggcct ggagggaaag tcccttggga cgatcataga gcgctagcac 660 tgaatcagcc tggagagcgc ggaaggaaag ggtcggtccg cagagggcgc ggggaaggca 720 gggtggggac gcggtggagc ccgcgctcgt ttgctgaagg cttggaagtg cagcgcagaa 780 gacagagggt gactaggaag acgcgcgagc ggggctggcc ggccggcggg tgggggaggg 840 gaggcggggg aaggcggctg agtgggcctc tggagtgtgt gtgtctgtgt cagtgtgtgt 900 gtgtgtgtgt gtatgtgtgt gtctggcgcc tggccagggt gatttcccat aaaccacatg 960 ccccccagtc ctctcttaaa aggctgtgcc gagggctggc cagtgaggct cggcccgggg 1020 aaagtgaaag tttgcctggg tcctctcggc gccagagccg ctctccgcat cccaggacag 1080 cggtgcggcc ctcggccggg 1100 // ID HSA_1437_CSF2 standard; DNA; HUM; 1100 BP. XX AC 1437; XX DT 06-Sep-2005 (Created) XX DE CSF2: colony stimulating factor 2 (granulocyte-macrophage) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 131436381..131437480 (FORWARD) CC Score Points: 51 (100.0%) CC Chromosomal Location: 5q31.1 XX CC Database Reference HGNC: 2434; CSF2 CC Database Reference ENTREZGENE: 1437 CC Database Reference UNIGENE: Hs.1349 CC Database Reference ENSEMBL: ENSG00000164400 CC Database Reference REFSEQ: NP_000749 CC Database Reference REFSEQ: NM_000758 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1400_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210229_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210229_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1401_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210229_s_at CC Database Reference TRANSFAC GENE: G000272; GM-CSF XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 131436381..131437480" FT /note="Genomic Strand: FORWARD" FT misc_signal 900..919 FT /note="TRANSFAC Site R00601" FT /note="TRANSFAC Site R00602" FT misc_signal 929..958 FT /note="TRANSFAC Site R05031" FT misc_signal 936..965 FT /note="TRANSFAC Site R04957" FT misc_signal 938..942 FT /note="TRANSFAC Site R00603" FT misc_signal 942..965 FT /note="TRANSFAC Site R05033" FT misc_signal 947..970 FT /note="TRANSFAC Site R05034" FT misc_signal 952..956 FT /note="TRANSFAC Site R00603" FT /note="TRANSFAC Site R00604" FT misc_signal 959..963 FT /note="TRANSFAC Site R00604" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP11137" FT misc_feature 1002 FT /note="SECONDARY ANCHOR: MMU [12981]; Alignment" FT prim_transcript 1004..>1004 FT /db_xref="ENSEMBL:ENST00000296871" XX SQ Sequence 1100 BP; 237 A; 308 C; 326 G; 229 T; 0 other; cattgtgaaa atcaaacact tgtcagcccc tcaagagcct ttagatttcc tacttccaca 60 cttccacaga aaggcctctg gagttggggg atgctggggt tatgtaggaa attaagcctg 120 gagggccttg ctggggaagc cattgtccct gtacctgaga tggatgcagc cacagccctg 180 gagccagcct gaagctcctg gtgtcttctg ggggctacat ataggagtgt agtccgaacc 240 tcagaggggc aaacctgctc tgcagaggga atcaaggttc acataaccag agaggggagt 300 cactcaggaa ggtggctcca gagccaagag tcagactctg ggtcccgact tgacccagcc 360 acaccccctc tgaagcttgc tgagagtggc tgcagtctcg ctgctggatg tgcacatggt 420 ggtcattccc tctgctcaca ggggcagggg tcccccctta ctggactgag gttgccccct 480 gctccaggtc ctgggtggga gcccatgtga actgtcagtg gggcaggtct gtgagagctc 540 ccctcacact caagtctctc acagtggcca gagaagagga aggctggagt cagaatgagg 600 caccagggcg ggcatagcct gcccaaaggc ccctgggatt acaggcagga tggggagccc 660 tatctaagtg tctcccacgc cccaccccag ccattccagg ccaggaagtc caaactgtgc 720 ccctcagagg gagggggcag cctcaggccc attcagactg cccagggagg gctggagagc 780 cctcaggaag gcgggtgggt gggctgtcgg ttcttggaaa ggttcattaa tgaaaacccc 840 caagcctgac cacctaggga aaaggctcac cgttcccatg tgtggctgat aagggccagg 900 agattccaca gttcaggtag ttcccccgcc tccctggcat tttgtggtca ccattaatca 960 tttcctctgt gtatttaaga gctcttttgc cagtgagccc agtacacaga gagaaaggct 1020 aaagttctct ggaggatgtg gctgcagagc ctgctgctct tgggcactgt ggcctgcagc 1080 atctctgcac ccgcccgctc 1100 // ID HSA_1439_CSF2RB standard; DNA; HUM; 1100 BP. XX AC 1439; XX DT 05-Sep-2005 (Created) XX DE CSF2RB: colony stimulating factor 2 receptor, beta, low-affinity DE (granulocyte-macrophage) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.22 35641722..35642821 (FORWARD) CC Score Points: 1 (100.0%) CC Chromosomal Location: 22q13.1 XX CC Database Reference HGNC: 2436; CSF2RB CC Database Reference ENTREZGENE: 1439 CC Database Reference UNIGENE: Hs.285401 CC Database Reference ENSEMBL: ENSG00000100368 CC Database Reference REFSEQ: NP_000386 CC Database Reference REFSEQ: NM_000395 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205159_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205159_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37494_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1086_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205159_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37493_at CC Database Reference TRANSFAC GENE: G003080; CSF2RB XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="22" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 35641722..35642821" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000262825" XX SQ Sequence 1100 BP; 203 A; 237 C; 368 G; 292 T; 0 other; tatatgtgta tatacatgta tgtatctgtg ttgttcatgt gtgtatgtgt gtctgtgtct 60 ctgtgtgtgt gtttgtatgt gtgtgtgcat gtttgtgtgt gtatatgtgt gtatattgta 120 tgtatctgtg tgtgtctgtg tctgcctctg tgtgtgtgtc tgtgtgtgca tttgtgtgta 180 tacatgtggg tatgtgtgtg catgttttgt gtgtacgtgt atatatgtat gtatctgtgt 240 gtgtctgtgt gttgtgcgtg tgtgtgcctg cgtgtgtccg tgtgcttgtg tgtgtgtgtg 300 tgtttgcatg ggcatcttga gtgaagcttc caacaatcta acagaagaaa aggagccaca 360 cttgtctgtt ctgctctctt gggtacttcc cagaccagtg aaatgaaagg gaggaaaccc 420 ccggcctccg aggagaaaag ggaactggca agcagagggt ggggggatga cggtaaaagg 480 agcaggggtg gggagagcac aggccctgtg gaagtgagga catgtgtgtg tacatgtgtt 540 catgtccagg ggatgacact gtggcatcca acagccgtgg accagcagcc cacggggagc 600 ttagtaggag tcaaatccta ggcccctgtc tcagctgctc tgctgtctag cgcattgtgc 660 agtggtaggt gtcagtgatc caagtgggga cccagtccct caggccacac agcgcatgtc 720 cattgccttc atgccgcagg agactgagag gtcatgcatg agggccactt ctctgggttg 780 tccccacaac acgggcggtg tccctgggac acgtggaagg ggaggggcag ctcactgctg 840 acatctcctt ctgcaggcct ggaggaggca gaggccagga gggagaggtc ccaagagcct 900 gtgaaatggg tctggcctgg ctcccagctg ggcaggaaca caggacttca ggacactaag 960 gaccctgtca tgcccatggc cagcacccac cagtgctggt gcctgcctgt ccagagctga 1020 ccagggagat ggtgctggcc caggggctgc tctccatggc cctgctggcc ctgtgctggg 1080 agcgcagcct ggcaggggca 1100 // ID HSA_1513_1_CTSK standard; DNA; HUM; 1100 BP. XX AC 1513_1; XX DT 06-Sep-2005 (Created) XX DE CTSK: cathepsin K (pycnodysostosis) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 147592222..147593321 (REVERSE) CC Score Points: 5 (6.4%) CC Chromosomal Location: 1q21 XX CC Database Reference HGNC: 2536; CTSK CC Database Reference ENTREZGENE: 1513 CC Database Reference UNIGENE: Hs.523594 CC Database Reference ENSEMBL: ENSG00000143387 CC Database Reference REFSEQ: NP_000387 CC Database Reference REFSEQ: NM_000396 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202450_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:128_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:129_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202450_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38466_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202450_s_at CC Database Reference TRANSFAC GENE: G009814; CATH-K XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 147592222..147593321" FT /note="Genomic Strand: REVERSE" FT prim_transcript 986..>986 FT /db_xref="dbTSS:WMD09079" FT prim_transcript 987..>987 FT /db_xref="dbTSS:MPB05973" FT prim_transcript 1008..>1008 FT /db_xref="dbTSS:MPC03469" FT /note="Number of reported TSSs: 2" FT prim_transcript 1015..>1015 FT /db_xref="dbTSS:MPC06423" XX SQ Sequence 1100 BP; 316 A; 223 C; 265 G; 296 T; 0 other; attacatgta aatggactat aagcaattgt gtaagccata tgtcatgctg caggctgcaa 60 attgttctta aaatggagga tttgtaatta agaaagccaa tgcaagaaat gagtgaagct 120 aactagagta aacttatgaa aagctgtgaa tttcatcatc atagaacatt gcttttcagt 180 ctgaacattc ttctaacaaa ccttggatct gaggcttctt gtcctttgcg gcagccacag 240 tgggtttttg ttgttagggg aaaaataaaa aaccttgccc gcagcatctg gttaagatta 300 gggcagtttc ctgcctaagg agggaaggga gagaaaaagg aagaagaaat gcataaggag 360 aatgaggaga tatacaatgt ctcagaaaac aggaaacatt gtcctatttt cccttgtcct 420 cttctgacaa gatctgggaa agtaccagaa tttaggcacg aaagagaaga acgcctcgaa 480 gaaatgatca ggaggcaaaa cttagacgga aatctctcct ttgtgtattc tgaaccccac 540 taccaccttg ctatttgtct gtctccaagc ctgctaggga ccctggagga aacgcactga 600 gcccattctg attgtccagt ttctatcccc catttctggt tgtgtacgtg tgtgtgtgtg 660 tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg tgagagagag agagacagag agagaaacag 720 agagagtgtg tgttgcctaa atctcccgag agagagagag agagagaaag agagaaatgg 780 ctaaatcccc ctagatcaaa gtccttggaa ccagatgtac cagcatccta tctaaacaca 840 ggcccctcct gactatcatt gttttatcac cctttttccg tctacctttc tcttcctcat 900 aaagcctagt tttcctctgt ttccctgcca aatggaagag ttttccctaa ctacattctt 960 ctgcaggatg tgggggctca aggttctgct gctacctgtg gtgagctttg ctctgtaccc 1020 tgaggagata ctggacaccc actgggagct atggaagaag acccacagga agcaatataa 1080 caacaaggtg cctggggtcc 1100 // ID HSA_1520_1_CTSS standard; DNA; HUM; 1100 BP. XX AC 1520_1; XX DT 06-Sep-2005 (Created) XX DE CTSS: cathepsin S XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 147518339..147519438 (REVERSE) CC Score Points: 13 (5.8%) CC Chromosomal Location: 1q21 XX CC Database Reference HGNC: 2545; CTSS CC Database Reference ENTREZGENE: 1520 CC Database Reference UNIGENE: Hs.181301 CC Database Reference ENSEMBL: ENSG00000163131 CC Database Reference REFSEQ: NM_004079 CC Database Reference REFSEQ: NP_004070 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41239_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202902_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:232617_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202901_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202901_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:65578_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202902_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202902_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:232617_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202901_x_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 147518339..147519438" FT /note="Genomic Strand: REVERSE" FT prim_transcript 799..>799 FT /db_xref="dbTSS:MPC00778" FT prim_transcript 860..>860 FT /db_xref="dbTSS:SYN04935" FT prim_transcript 870..>870 FT /db_xref="dbTSS:MPB08335" FT prim_transcript 888..>888 FT /db_xref="dbTSS:LNG03345" FT prim_transcript 899..>899 FT /db_xref="dbTSS:LNG08658" FT prim_transcript 929..>929 FT /db_xref="dbTSS:MPE08718" FT prim_transcript 1077..>1077 FT /db_xref="dbTSS:MPB07923" FT prim_transcript 1085..>1085 FT /db_xref="dbTSS:MPC02348" FT prim_transcript 1086..>1086 FT /db_xref="dbTSS:MPG08282" XX SQ Sequence 1100 BP; 340 A; 205 C; 198 G; 357 T; 0 other; acatctctaa caagtagcct ctgctgcaga gtaggtaagg aatacaggtg catgccacca 60 tgcctggcta attaaaaaaa aatttttttt gtagaatcag ggacttgcta ttttgcccag 120 gctgctctca aactctggcc tcaaacaatc ctcccacttc agcctctcaa agcacttgga 180 ttacaagtgt gagccaccat gcctggctca tttttcaata gctttaatta tgagaaagtc 240 agctccactt ctagatcaaa aagctctttc agagctgcat ttttgttgtt tgctttagaa 300 ttccctgccc tatacctttt tcatagtagt cactcaaaaa tatttcttaa ttgacattct 360 ctagaggaat ttaagtttga tagaaaatca ttacacatga tactgttatc aaaaaattta 420 gagataaagg cttataaagg atactaatac tctttcttta gagaaggcat atttgcaaag 480 taggaggatt aaaggactgg gatggatctt actatagttt tccttaggta ttaagtctat 540 tcatcaatat agcactaaag ctttccaaac cattattttg agttacctga aatccctgga 600 gaaattatta ccttatttca ttctaatttt gttttacggc ctttcatatg taatcactta 660 taggagaaaa acaatgagat aaaaagttga taacatggtt tgattgtacg catttgtaat 720 tttgtattat ttctttttct aaagctgggg ccacaacttt ggtgaagaag gatatattcg 780 gatggcaaga aataaaggaa atcattgtgg gattgctagc tttccctctt acccagaaat 840 ctagaggatc tctccttttt ataacaaatc aagaaatatg aagcactttc tcttaactta 900 atttttcctg ctgtatccag aagaaataat tgtgtcatga ttaatgtgta tttactgtac 960 taattagaaa atatagtttg aggccgggca cggtggctca cgcctgtaat cccagtactt 1020 gggaggccaa ggcaggcata tcaacttgag gccaggagtt aaagagcagc ctggctaaca 1080 tggtgaaacc ccatctctac 1100 // ID HSA_1540_CYLD standard; DNA; HUM; 1100 BP. XX AC 1540; XX DT 06-Sep-2005 (Created) XX DE CYLD: cylindromatosis (turban tumor syndrome) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.16 49332503..49333602 (FORWARD) CC Score Points: 2 (22.2%) CC Chromosomal Location: 16q12-q13 / 16q12.1 XX CC Database Reference HGNC: 2584; CYLD CC Database Reference ENTREZGENE: 1540 CC Database Reference UNIGENE: Hs.432993 CC Database Reference ENSEMBL: ENSG00000083799 CC Database Reference REFSEQ: NP_056062 CC Database Reference REFSEQ: NM_015247 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:221903_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:214272_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:221905_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:221903_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:221905_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:214272_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:214272_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:221905_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:221903_s_at CC Database Reference TRANSFAC GENE: G009286; CYLD XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="16" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 49332503..49333602" FT /note="Genomic Strand: FORWARD" FT misc_feature 232..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT prim_transcript 984..>984 FT /db_xref="ENSEMBL:ENST00000311559" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [74256]; Alignment" FT misc_feature 1011 FT /note="SECONDARY ANCHOR: MMU [74256]; Alignment" FT prim_transcript 1017..>1017 FT /db_xref="ENSEMBL:ENST00000338118" XX SQ Sequence 1100 BP; 230 A; 315 C; 322 G; 233 T; 0 other; ccttctccta taattagcac ttaaaatgtc aaaggagaag aaattaatta acaggagtat 60 ccagtgcagc aaggctctag gactgattat aaaaagcact tccttaaata ttttgagtgc 120 ttttgggaat cagaagcctc ccttctaatt gaaagatcct taactacacc ctaagtcctg 180 gctggtggcc aggggtgcgg ggctgagtga ggcggcgtgt ggaaatccct tcttcaccat 240 ccttgggaaa attccctcca aactgggata ggtggcaaca gaggttcgga aacagcaagc 300 gtcccaggct gaatctgcgg aggaggaaga gatgaacctt tcctgagctg gtactgcgtg 360 ccaggaactt tagctcggta ttttgccaca atcctgtaag acaaccgata ctatgatctc 420 cattttacag atgaggacat tgaggctcag cgtggttgtg acttcctcag gtcacgcagc 480 cactgaatga aagcgccaaa gattcaaact gaggtctgat tctaaagctt tgctctctca 540 cggcatcctg gaatcctatt tcaaccttca tctggactct taacccagcc caaacctaag 600 cgtctacagt tttgacagct gaggcgggag cacgggaggc ggagctggtg gcagcgcagc 660 gccccgcccc ggctccagca tcagccaatg gtgacgcggc acccacagcc tttcgcccaa 720 tcagcttgag cttcccgcct ccatccgccg ctcttctctg ccccgcccct tcgctttccc 780 tttggttcca ccgagcttga cagagcggaa agtcccttcg gccggcgccg ggctggcagc 840 cattggagga aggtctgtca cagggaggcc caatcacggc ccgctcagga gcgcagctcg 900 gcctacgatt ggctagcgcg gcggctgccc cctccgcccc cgctccctcc ctcttccctg 960 tgcggttcgg aggcggggca ggtgggggcg ggcccaggta gcaggtttgg ctgcgcgggg 1020 gccgcgcgtc ggaggtaaat actagggcgg tgggtgtggg gagccggggc cggcccggga 1080 cgcgggctgg ggagccgggg 1100 // ID HSA_182_JAG1 standard; DNA; HUM; 1100 BP. XX AC 182; XX DT 07-Sep-2005 (Created) XX DE JAG1: jagged 1 (Alagille syndrome) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.20 10602537..10603636 (REVERSE) CC Score Points: 1 (16.7%) CC Chromosomal Location: 20p12.1-p11.23 XX CC Database Reference HGNC: 6188; JAG1 CC Database Reference ENTREZGENE: 182 CC Database Reference UNIGENE: Hs.224012 CC Database Reference ENSEMBL: ENSG00000101384 CC Database Reference REFSEQ: NM_000214 CC Database Reference REFSEQ: NP_000205 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209097_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209097_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209098_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209098_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:74827_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33178_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209098_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35414_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209099_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209099_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:216268_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209097_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:216268_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:216268_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209099_x_at CC Database Reference TRANSFAC GENE: G006326; JAG1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="20" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 10602537..10603636" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000254958" XX SQ Sequence 1100 BP; 147 A; 424 C; 361 G; 168 T; 0 other; ctgccacccc agagaaggca agttccgcgg ctggcggtgc tggggacacg gtccctccca 60 ggcccatctc ttgccaccca gagagctgct cggaggccgc ctacaggtgc aatcccggca 120 ctgcggccgg ggcgtcgggc cggggagggc gtccaagccc accagcatct ccgccggccc 180 ttcccaaagc ctgaacaggg ccccggcgtg cccgccgcct tctacccccg gtttccccgc 240 gcctctgccc cggcgcggtt tggataggaa gctgggagcc ctcccaggct ccgcagactc 300 ggatttggga gggggtggga cgcggccgag gcttcccctc gaatctgcgg caagcctggc 360 tccaggaaag tttttcaaag ttcccagcag cgtctgccca ggtcgcctcc gcggggcgag 420 cagacggcgg caagcgcgcc agcctcgccg ccgcctctgc cgccagcaga gcgctctggg 480 cggctcgctc gcgggaagcg ggccgaactc ccggcgggca ggcaggccct cctcccgggg 540 cgaaagccgc agctgacgca ggcggttcgg aaggcggaag ctgccccgct ccgaccgctc 600 agtcagcgcc gcggcgccta cacctggggc cccgacgcgc gggcaaaggc gcacggcccg 660 gggcgcccga gggggcggtc cccgctgggg gcctccaggc gtccctgagc aacgatccct 720 tccaagtacc tccccgcact ctcccttccc tcctggcccg aagctcccga gggcgggggt 780 tggtgtgggg ccctggttct tctacgccgc cctgagcatc ccgctgcccc caaccccttc 840 caagttcctc ctcgcactac cccctcccca gcaacgtgaa ggggaggggc gtgcccaggg 900 tgagcacgcc ctctcatgaa tattaataag cgcgcatgcg ccctgcccgg cgtgctgggt 960 agaggtggcc agccccggcc gctgctgcca gacgggctct ccgggtcctt ctccgagagc 1020 cgggcgggca cgcgtcattg tgttacctgc ggccggcccg cgagctaggc tggttttttt 1080 ttttctcccc tccctccccc 1100 // ID HSA_1942_EFNA1 standard; DNA; HUM; 1100 BP. XX AC 1942; XX DT 05-Sep-2005 (Created) XX DE EFNA1: ephrin-A1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 151912430..151913529 (FORWARD) CC Score Points: 27 (93.1%) CC Chromosomal Location: 1q21-q22 XX CC Database Reference HGNC: 3221; EFNA1 CC Database Reference ENTREZGENE: 1942 CC Database Reference UNIGENE: Hs.516664 CC Database Reference ENSEMBL: ENSG00000169242 CC Database Reference REFSEQ: NM_004428 CC Database Reference REFSEQ: NP_872626 CC Database Reference REFSEQ: NP_004419 CC Database Reference REFSEQ: NM_182685 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202023_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202023_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40425_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202023_at CC Database Reference TRANSFAC GENE: G003082; EFNA1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 151912430..151913529" FT /note="Genomic Strand: FORWARD" FT prim_transcript 580..>580 FT /db_xref="ENSEMBL:ENST00000303357" FT prim_transcript 980..>980 FT /db_xref="dbTSS:RCT04918" FT prim_transcript 983..>983 FT /db_xref="dbTSS:HRC11081" FT prim_transcript 993..>993 FT /db_xref="ENSEMBL:ENST00000335075" FT prim_transcript 994..>994 FT /db_xref="dbTSS:HPR04735" FT prim_transcript 995..>995 FT /db_xref="dbTSS:REC07262" FT /note="Number of reported TSSs: 2" FT prim_transcript 996..>996 FT /db_xref="dbTSS:ADB07576" FT /note="Number of reported TSSs: 9" FT misc_feature 996 FT /note="SECONDARY ANCHOR: MMU [19729]; Alignment" FT prim_transcript 998..>998 FT /db_xref="dbTSS:RCT02769" FT /note="Number of reported TSSs: 2" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:HRC08316" FT prim_transcript 1016..>1016 FT /db_xref="dbTSS:NRB06373" FT /note="Number of reported TSSs: 2" FT prim_transcript 1022..>1022 FT /db_xref="dbTSS:HRC09396" FT prim_transcript 1025..>1025 FT /db_xref="dbTSS:RCT01302" FT prim_transcript 1027..>1027 FT /db_xref="dbTSS:HRC00591" FT prim_transcript 1028..>1028 FT /db_xref="dbTSS:HSI15174" FT /note="Number of reported TSSs: 2" FT misc_feature 1034 FT /note="SECONDARY ANCHOR: RNO [94268]; Alignment" FT prim_transcript 1037..>1037 FT /db_xref="dbTSS:PNC05427" XX SQ Sequence 1100 BP; 232 A; 373 C; 309 G; 186 T; 0 other; gctgcacgcc ggtacgcgtc tcccctcctc ttcacacgct gttcacaaac attagcatac 60 gtctgtcaaa gagtttcaca cgcttccaca cacgcggctg tgatactact cacaaatgct 120 ttcatgctag cgcgccatca cacgtatttc atgtgtggtt acagtttgtc acccttcatg 180 cccagattct cacagtccat attcaagagc ctgttcgcac ggtgtacgcg tgtgttgtta 240 catatactca ggttattagc gctctttgac ttatctaaaa taagaacggc cccctctcga 300 gcccagggtc ccgcgtgtcg ctcctgcggg caggcactga tgtgatggac agaggcgtcc 360 ttagccccgg ccgcacacgt tacacactcg atcacacaaa gcgttgcact ttattcccgg 420 catctaggcg atgacacaat ctccagaaca aagacaacat tgacaaaccc aacaaaaaca 480 aacagccgcg tgtgtgtggg gaggggcagt caagcgcaga gtccgggaag gggatggggg 540 aggaggagag tgtgggaacg cgggcgcccg agcctgggca tgcgaggctc agaaaggtgc 600 ggggcatgtc aacaacctcg caccctgcaa ggtccgcgcg cggagcagca aagccgtgtc 660 ccgcaccccc gcgttcgcag actcgcactt gcgagttctt cccttctccc gcacgcgact 720 gcgcccaggg acgcaagccc accaccggga caggctcaca aagctccacg cagacccaca 780 agtgagcgaa cacacatctc tgagcagatc tgcgggggca gaggagcgcg cttcgctctt 840 tcctgcaccc ccagcctcct cgcctcccca ccccgcccct cctccacctc cccagccccc 900 aagcccccag gcagccgcgc gccgggcggg gcgagggcgg ggcggggtgt cgggcggcgc 960 cggcccaaaa ggcggagtcg ctaggcgaag gggccagatc tgtgagccca gcgctgactg 1020 cgccgcggag aaagccagtg ggaacccaga cccataggag acccgcgtcc ccgctcggcc 1080 tggccaggcc ccgcgctatg 1100 // ID HSA_2113_ETS1 standard; DNA; HUM; 1100 BP. XX AC 2113; XX DT 05-Sep-2005 (Created) XX DE ETS1: v-ets erythroblastosis virus E26 oncogene homolog 1 (avian) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.11 127897285..127898384 (REVERSE) CC Score Points: 3 (100.0%) CC Chromosomal Location: 11q23.3 XX CC Database Reference HGNC: 3488; ETS1 CC Database Reference ENTREZGENE: 2113 CC Database Reference UNIGENE: Hs.369438 CC Database Reference ENSEMBL: ENSG00000134954 CC Database Reference REFSEQ: NM_005238 CC Database Reference REFSEQ: NP_005229 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:214447_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:57073_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:214447_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1518_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:224833_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1977_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:224833_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1555355_a_at CC Database Reference TRANSFAC GENE: G000217; c-ets-1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="11" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 127897285..127898384" FT /note="Genomic Strand: REVERSE" FT prim_transcript 972..>972 FT /db_xref="dbTSS:TIR06208" FT prim_transcript 1014..>1014 FT /db_xref="ENSEMBL:ENST00000319397" FT prim_transcript 1016..>1016 FT /db_xref="ENSEMBL:ENST00000345075" XX SQ Sequence 1100 BP; 230 A; 338 C; 344 G; 188 T; 0 other; ggttcccaaa tggaacagaa actgtgcatt gtgattctgt catggctgcc aatgatgtac 60 tccagaaatt caaaaccaca gagcctctgc atcacttttt tggtggcggt cgtgggaggg 120 ttgttagttt tatctaaaag aggagagtct gtgaaaggaa agacaaagct ttggccaatg 180 gtgacataat tagaggaaca gaataattag aaataaatca taacttcccc ttcaacccaa 240 ccactgctgg aggtaaattg gaagcttacg gaagctcatg gctgggttct agtttggggt 300 cccgttctgg actcccctgc caacgcagga gcattacatg ggtgggctct gaaaaactga 360 agcctccttc agaaacacac gccctgactc aagatccggc tggagtccaa tactcctaaa 420 gccctttgag gacacgggct cacgaatccc ctgcgcctgc ctgcacgctc gccttcatcc 480 acatgcctca cgtcctgtgt gtcagtcttt gtgaatgaat gatgtacacg cacttggaaa 540 actatgctgc tactgggagg gggcgagagc gggtgaccaa gccctcaaga atgcgtggag 600 aatcagacgg actttcccga aacggtggag gcggcctgtg cacccagcct gcacacccgc 660 tcccggccct tcccgcccct gcctgggctc cgaggcccgg ggctccacgc actgctcctc 720 cgcggtcgcg gcccggcccc gcgctcgcca gcccttcctt tcgctttggg ccgcgggcgg 780 agattggccg cggtgctcgg ccccgccccc ggctccccgc cctgccccga cgccccgccc 840 ctcgctcccc caagcggaca tcgcccggcc cagggcgcgc ggacccagcg gccgagacgc 900 ggcgccgcga gaaacgccct aaagaggagg ggagagcgcg ggagggcgag agggagggag 960 agcggccggg agatcgagag cgaacgaggc agccgccggc ggagaggagg gagcgggcga 1020 gggccgggca ggaggagcgg gcgcggcgcg ggcgaggctg ggacccgagc gcgctcactt 1080 cgccgcaaag tgccaacttc 1100 // ID HSA_2152_F3 standard; DNA; HUM; 1100 BP. XX AC 2152; XX DT 05-Sep-2005 (Created) XX DE F3: coagulation factor III (thromboplastin, tissue factor) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 94719238..94720337 (REVERSE) CC Score Points: 25 (96.2%) CC Chromosomal Location: 1p22-p21 XX CC Database Reference HGNC: 3541; F3 CC Database Reference ENTREZGENE: 2152 CC Database Reference UNIGENE: Hs.62192 CC Database Reference ENSEMBL: ENSG00000117525 CC Database Reference REFSEQ: NP_001984 CC Database Reference REFSEQ: NM_001993 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36543_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204363_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204363_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204363_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 94719238..94720337" FT /note="Genomic Strand: REVERSE" FT prim_transcript 957..>957 FT /db_xref="ENSEMBL:ENST00000334047" FT prim_transcript 975..>975 FT /db_xref="dbTSS:COL03779" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [14066]; Alignment" FT /note="PRIMARY ANCHOR: RNO [25584]; Alignment" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:T7R06129" FT /note="Number of reported TSSs: 9" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:TIR00519" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:T7R07336" FT prim_transcript 1005..>1005 FT /db_xref="dbTSS:T7R00193" FT /note="Number of reported TSSs: 10" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:STM00892" FT prim_transcript 1008..>1008 FT /db_xref="dbTSS:T3R05339" XX SQ Sequence 1100 BP; 208 A; 356 C; 335 G; 201 T; 0 other; aagtttacag caaagcccag aaggagaagc cagaaaataa tttagaaaaa ccaaagctta 60 aaactagtgg cacacaactc tggttacatt tttcattttc atttttggtt cctctgcatt 120 tcggtggaac tcagtcccac agatgtcttc ttcaatgtgg gaaccatcct ttctggaacc 180 acagagctgc agatgtcacg ctggaattct cccagaggca aactgccaga tgtgaggctg 240 ctcttcctca gtcactatct ctggtcgtac cgggcgatgc ctgagccaac tgaccctcag 300 acctgtgagc cgagccggtc acaccgtggc tgacaccggc attcccaccg cctttctcct 360 gtgcgacccg ctaagggccc cgcgaggtgg gcaggccagg tattcttgac cttcgtgggg 420 tagaagaagc caccgtggct gggagagggc cctgctcaca gccacacgtt tacttcgctg 480 caggtcccga gcttctgccc caggtgggca aagcatccgg gaaatgccct ccgctgcccg 540 aggggagccc agagcccgtg ctttctatta aatgttgtaa atgccgcctc tcccacttta 600 tcaccaaatg gaagggaaga attcttccaa ggcgccctcc ctttcctgcc atagacctgc 660 aacccaccta agctgcacgt cggagtcgcg ggcctgggtg aatccggggg ccttggggga 720 cccgggcaac tagacccgcc tgcgtcctcc agggcagctc cgcgctcggt ggcgcggttg 780 aatcactggg gtgagtcatc ccttgcaggg tcccggagtt tcctaccggg aggaggcggg 840 gcaggggtgt ggactcgccg ggggccgccc accgcgacgg caagtgaccc gggccggggg 900 cggggagtcg ggaggagcgg cgggggcggg cgccgggggc gggcagaggc gcgggagagc 960 gcgccgccgg ccctttatag cgcgcggggc accggctccc caagactgcg agctccccgc 1020 accccctcgc actccctctg gccggcccag ggcgccttca gcccaacctc cccagcccca 1080 cgggcgccac ggaacccgct 1100 // ID HSA_23264_ZC3H7B standard; DNA; HUM; 1100 BP. XX AC 23264; XX DT 07-Sep-2005 (Created) XX DE ZC3H7B: zinc finger CCCH-type containing 7B XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.22 40021086..40022185 (FORWARD) CC Score Points: 11 (78.6%) CC Chromosomal Location: 22q13.2 XX CC Database Reference HGNC: 30869; ZC3H7B CC Database Reference ENTREZGENE: 23264 CC Database Reference UNIGENE: Hs.474970 CC Database Reference ENSEMBL: ENSG00000100403 CC Database Reference REFSEQ: NP_060060 CC Database Reference REFSEQ: NM_017590 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213323_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35144_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213323_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205877_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205877_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205877_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213323_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="22" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 40021086..40022185" FT /note="Genomic Strand: FORWARD" FT prim_transcript 949..>949 FT /db_xref="dbTSS:CAE09141" FT prim_transcript 982..>982 FT /db_xref="ENSEMBL:ENST00000351589" FT /note="Number of reported TSSs: 2" FT prim_transcript 993..>993 FT /db_xref="dbTSS:KGR06775" FT /note="Number of reported TSSs: 3" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:OFR00331" FT prim_transcript 1005..>1005 FT /db_xref="dbTSS:OFR04952" FT prim_transcript 1006..>1006 FT /db_xref="dbTSS:OFR08691" FT prim_transcript 1031..>1031 FT /db_xref="dbTSS:ADG08654" FT prim_transcript 1080..>1080 FT /db_xref="dbTSS:HPR00965" XX SQ Sequence 1100 BP; 252 A; 317 C; 285 G; 246 T; 0 other; ctgcctcagc ctcctgagta gctgggatta caggcaccca ccaccacgcc tggctaattt 60 ttgtattttt gtagagatgg ggtttcacca cgttggctag tctggtcttg aactcctgac 120 ctcaggtgat ccacccgtct tggcctccca aagtgctgag attacaggcg tgagccactg 180 cacccagccc tgattgtcaa tatctaatca ggttcctcat tttccaccat tccccaggtg 240 atgtctgatc accttgccct gccttcagca agaatcttgt tagatgggtt taagcgagaa 300 tcctctcatc tctgatgcag tttcctatgc actggcgctc aatcagtgga tcctttctcc 360 ttcctcataa attcccagtt gcccatgctg atttctgaat tgagcccaaa tactctccct 420 gaccgcaaaa cccactgcag tggtccctac acccatcatg atgccaataa agtcggcctt 480 gtagtcttta acaagtgtca ttcaatattt tttttaacat cctatacata aaactccagc 540 caagtgaggt cctgattctt ctatgtgtct ccggttccca tctatgagaa gggcacaacg 600 caaccagggt tttgggcagc cttccatgaa agcacctgga agccggagaa ggggggcggg 660 gggacttttg acacagatgg ggaagggcgg aggcgctggg tttgagcagc atcagcccag 720 aaatgcagaa ctgccaaaag aaacccccct aaaaggcagg acacttttaa agaaaataaa 780 ggtgaattcc aggcatgagc tttcgacggg gaatggggct tccccgactc gcccccacgc 840 cccccgccct tctccccagg tgcgcagccc gcgccgccca ccccgggcgc ggcgaggcga 900 cgggagccga gctctctagg acccgaggag gaagagctgc agggagacag tgcctccagc 960 gggtgctgcc gcgagcggcc agccgagggg ctggaaatga aagtaaagcg ctccagagcc 1020 acatggacgg agctgccggg gcggcggcgc cgggagcagg atgcggccgc ccgtaattaa 1080 atagcattta ctcttattat 1100 // ID HSA_23308_ICOSLG standard; DNA; HUM; 1100 BP. XX AC 23308; XX DT 07-Sep-2005 (Created) XX DE ICOSLG: inducible T-cell co-stimulator ligand XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.21 44485101..44486200 (REVERSE) CC Score Points: 2 (100.0%) CC Chromosomal Location: 21q22.3 XX CC Database Reference HGNC: 17087; ICOSLG CC Database Reference ENTREZGENE: 23308 CC Database Reference UNIGENE: Hs.14155 CC Database Reference ENSEMBL: ENSG00000160223 CC Database Reference REFSEQ: NM_015259 CC Database Reference REFSEQ: NP_056074 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213450_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213450_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211199_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211198_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:31803_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211197_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213450_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211199_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211198_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211197_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211199_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211197_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211198_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="21" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 44485101..44486200" FT /note="Genomic Strand: REVERSE" FT prim_transcript 952..>952 FT /db_xref="ENSEMBL:ENST00000291579" FT prim_transcript 1050..>1050 FT /db_xref="ENSEMBL:ENST00000344330" XX SQ Sequence 1100 BP; 149 A; 412 C; 377 G; 162 T; 0 other; cctgtctagc agcctcaccc aggcccttcc ggaggtgcct ctgcagaaag ggagtcacgt 60 cccccctggg cctcacctgg cttgcaggga tcagggaggg agggcggggt gggctgggtg 120 cggtggggaa ggagcaggga ctctgggtcc caccctcggt tgcgtggtgc agcctttccc 180 aaaccagctg ccccagactc caggccagac gccactgcca aggctgacga gcccagagcc 240 gcaagcctgc ctcggtttct cggcggggga tcctcagagc cagtgttaag caaagaggct 300 gcgccagcgc ccttcacacc cctagaaggc taggggagca aggctaggtg ggggcgggct 360 ggggctggcc cagagggtag agcccgccca ctttccctcc ctccttccat tcatgcatgc 420 gttcattcag tcattcattc ctcagcagtc gctgagctca ctcgccttaa gtcctggaga 480 tcatcggagc gcagccggcc aggggcctgg cgctctccca gccttggggc ctgggtcccc 540 ggactcctgc tcggggaggg ccgcaggacc ggcgcattgt gcgcggcgcg gggaacggcc 600 cttgcctccc acggtgccct ccctcgctgc gccggcaccc gcagcacccc tggccacctt 660 cctgccgggt accccccacc cctgcgcttc ccagggcacc tacggcgccc aggtccgcgt 720 ccaggcggac aggccgacct gcctctgtcc cgcctccggc cgacgggcac acgcctgggc 780 agagccgaac tttccggagc cgccgcgcag cgccccgcct cctgtcccgg ggcggtctcg 840 gtcgccagag gagccaggcc gggggcgggg cggggacggg gcggggacac ggctgcctcc 900 agcacaccgc gcgctgggcg ctcagagcct cgggcgcggc gggagcgcag ttagagccga 960 tctcccgcgc cccgaggttg ctcctctccg aggtctcccg cggcccaagt tctccgcgcc 1020 ccgaggtctc cgcgccccga ggtctccgcg gcccgaggtc tccgcccgca ccatgcggct 1080 gggcaggtga gccggggaag 1100 // ID HSA_23586_1_DDX58 standard; DNA; HUM; 1100 BP. XX AC 23586_1; XX DT 07-Sep-2005 (Created) XX DE DDX58: DEAD (Asp-Glu-Ala-Asp) box polypeptide 58 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.9 32447057..32448156 (REVERSE) CC Score Points: 3 (11.5%) CC Chromosomal Location: 9p12 XX CC Database Reference HGNC: 19102; DDX58 CC Database Reference ENTREZGENE: 23586 CC Database Reference UNIGENE: Hs.190622 CC Database Reference REFSEQ: NM_014314 CC Database Reference REFSEQ: NP_055129 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:218943_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:222793_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:218943_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:76098_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:77749_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:59215_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:222793_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:242961_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:242961_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:218943_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="9" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 32447057..32448156" FT /note="Genomic Strand: REVERSE" FT prim_transcript 913..>913 FT /db_xref="dbTSS:LNF01034" FT prim_transcript 998..>998 FT /db_xref="dbTSS:kaia4495.seq" FT prim_transcript 1092..>1092 FT /db_xref="dbTSS:WMC06337" XX SQ Sequence 1100 BP; 270 A; 224 C; 236 G; 370 T; 0 other; ggctgggctg gctcagatga ggagttatta cttcaggatg ttccgttcgt cttcagaaag 60 cagaaatctc tcatcagctc agctgtttgg gcaaaaagcc tattaggagt catattgcta 120 agttccctta cctttctaag tctgcttctt tagctgtaaa aggtcctttc agctccaatt 180 tgggtgattg ttctactaaa aatggccctt ttagacccta tgttttcctg agggactagt 240 atgttggatc tgcatttgtt tctgagctgt ttactctaaa gttgactcta ggtggggcct 300 gtggacacat tagtccctga ccttcttcaa ttgcatcttg accttggtcg ttttccctgt 360 atcctttgga ttgtgcctgc cagggccact ggtgaacttc agcttcacaa attttcagca 420 aacatcgctt ctgtttttga ataatgagta tctaccttca gaagctgggt tacctggaac 480 cttcttaatc ttcttcttta tgaggtgccc agtgtcctca cttgcaaccc caccctgcct 540 gtagagggga gtcaggtgca tggatcctct ggactttggg tgaatctatt tttttttttc 600 ctccaattgt aaaataagtg agacccacct gttctttgcc tcagattatt gtggggtttt 660 cttttttttt tttttaaatc acaattatgt actggttcta acgttctctt ttgtgtgtta 720 ttccatccct tcatctgtag gaatgccatt acactgtgct tggagatgct tttaaggaat 780 gctttgtgag tagaccacat cccaagccaa agcagttttc aagttttgaa aaaagagcaa 840 agatattctg tgcccgacag aactgcagcc atgactgggg aatccatgtg aagtacaaga 900 catttgagat tccagttata aaaattgaaa gttttgtggt ggaggatatt gcaactggag 960 ttcagacact gtactcgaag tggaaggact ttcattttga gaagatacca tttgatccag 1020 cagaaatgtc caaatgatat caggtcctca atcttcagct acagggaatg agtaactttg 1080 agtggagaag aaacaaacat 1100 // ID HSA_24145_PANX1 standard; DNA; HUM; 1100 BP. XX AC 24145; XX DT 05-Sep-2005 (Created) XX DE PANX1: pannexin 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.11 93500742..93501841 (FORWARD) CC Score Points: 1 (12.5%) CC Chromosomal Location: 11q21 XX CC Database Reference HGNC: 8599; PANX1 CC Database Reference ENTREZGENE: 24145 CC Database Reference UNIGENE: Hs.503584 CC Database Reference ENSEMBL: ENSG00000110218 CC Database Reference REFSEQ: NM_015368 CC Database Reference REFSEQ: NP_056183 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35623_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:236372_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204715_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204715_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:236372_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:51075_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204715_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:80145_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="11" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 93500742..93501841" FT /note="Genomic Strand: FORWARD" FT misc_feature 932 FT /note="SECONDARY ANCHOR: MMU [55991]; Alignment" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000227638" XX SQ Sequence 1100 BP; 231 A; 327 C; 287 G; 255 T; 0 other; agaacactga cttgtttctg aatcatataa actttgattt tcttgtgcac aaaacatttt 60 agcctgtatg ttgtcatctg cagccagtga ctgtaacctg tgtaccatac cctccgatga 120 aaaaaatccc acctctgata taaggggtcc tcctcccttt tcctaaactt tcttctaaaa 180 cccttccaac gtgtaacaaa ttttgaaaca tgcccaactt tgctggtaag tcttcttggg 240 tggatcctca catttagctt ccaataaatc aaattatttc tacttcaaca gccttaattt 300 ccgtggacac tggtcagagt atttcctcct gtctttccat catccacttc ctatgagctg 360 ttcagaagca gctctctgca gccccaacac ccacctacct gcaggccccc ctctctctgc 420 tggctcccgg aacaaggctc tgattgggat ggcagaggaa agagaaacgg gaccagcagc 480 gctactcagg cctcgaaact ccacactcac taccgtttcc gcgccaccct ctcacgcgga 540 gctcctggaa gggtccagcg ctccctctgc aaggcaccgt cggtctacac cgctcgattg 600 gccttttatg gcactgactg ttctttgaag cttttgcagc tccttctaac ccgatttcac 660 cgtgttggaa atgttggggg tggggcgtaa agggggccat cccatccaca gaaagagtcg 720 cttgcagaaa tgattttaaa actcccgggt gccaggacgt gaggagaatc cggcagggag 780 ggacgggaga atttccaaag gtgccgctca gtgggaaaat ccctttgtca gagagtggcc 840 cgaggggcgc ggaatgcagc cgcgcccacc ccgccccgcg tcaccgcgtc ttccggaagc 900 tccacgcccc tgggtacttg gtttccccgc atggttccgg aagagcgcgg cgcagctggc 960 tgtgagcgca gggctatccc ggcggccgct tcggcagcca gggcggcgcg gaggggcagg 1020 gccagaggga agcgctttgt tccgcgcgtg gttcccgcgc ctgggggtgc gcgggagagg 1080 cgcgaatccg agtgccgcgc 1100 // ID HSA_2550_GABBR1 standard; DNA; HUM; 1100 BP. XX AC 2550; XX DT 06-Sep-2005 (Created) XX DE GABBR1: gamma-aminobutyric acid (GABA) B receptor, 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 29708740..29709839 (REVERSE) CC Score Points: 3 (33.3%) CC Chromosomal Location: 6p21.31 XX CC Database Reference HGNC: 4070; GABBR1 CC Database Reference ENTREZGENE: 2550 CC Database Reference UNIGENE: Hs.167017 CC Database Reference ENSEMBL: ENSG00000197402 CC Database Reference REFSEQ: NP_006389 CC Database Reference REFSEQ: NP_068704 CC Database Reference REFSEQ: NP_068705 CC Database Reference REFSEQ: NP_001461 CC Database Reference REFSEQ: NM_021905 CC Database Reference REFSEQ: NM_021903 CC Database Reference REFSEQ: NP_068703 CC Database Reference REFSEQ: NM_001470 CC Database Reference REFSEQ: NM_006398 CC Database Reference REFSEQ: NM_021904 CC Database Reference AFFYMETRIX: AFFY_HG_U95D:82572_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:238629_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:86077_i_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205890_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203146_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205890_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:90032_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:238531_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203146_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32623_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205890_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:238531_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39959_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203146_s_at CC Database Reference TRANSFAC GENE: G003245; GABBR1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 29708740..29709839" FT /note="Genomic Strand: REVERSE" FT misc_feature 113..959 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000306809" FT /note="Number of reported TSSs: 3" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [54393]; Alignment" XX SQ Sequence 1100 BP; 163 A; 436 C; 247 G; 254 T; 0 other; cccccaacaa ggagcccact gtttcctctc ccagcccaaa ctcaggccta cgaacaacaa 60 cagcacaaca cacacacaca cacacacaca cacacacaca cacacacaca cacacacccc 120 tccacttcaa ggtatagcca agagcttctg gagccgtcaa aaaggtctgt acctgctgtc 180 tttagagctt ccagtttgcc cttggtcaag aaatactgtt tgctaggctc tgctggagta 240 catcaggtaa tactggcttc taaaccaccc tgaggttctt ttctcttgtc cttttactcc 300 cttcgtactt caatttctct ccttgatgtc cccctccctg ttttgttttt tgcctccaat 360 ccgttctgcg cgttccctgc agagcaggcg agtagcaatg ctgctggacc atggagctgc 420 tctagtctcc cagaaatctc ttctacaccc aacccttctt gcgcttaggt ggtcctcagt 480 ccccctcccc cacctccttc tgacccaggc ttctttctcg ccctccggtc gcagttctcc 540 tgggcatctg cctctgcctc tctcctctca cccggatcta gggctgcctt ctctttgtgc 600 agccgtcttt ctccaccttc atcccagact ccctgtctca gcgccagctc ctctgccttt 660 ggctcgggtt ccctctcccc caccccagct tccagttgtt tggcccgcag gtccctcggc 720 agtgaccggc gccccccgac gagtgcgtgt gcaccagggc acctccctct cccccacctc 780 tcagccccgc gcctctccac cgcccgcccc accgcgctgt gggcggtcca gggcggggct 840 gggatccggg gcggctcccg gggctcgggt tgtgggaggc gccctctccc cggtcttccc 900 ctctcttccc cccgccctgc cttcccttgc accctccttc ttccctccgc ccgggagctc 960 tccctggtcc ccggcgccgc ctccttccct cccggctccc cgctccccgc tcccgtggct 1020 gccgccgccc cggggaagaa gagacagggg tggggtttgg gggaagcgag agaggagggg 1080 agagaccctg gccaggctgg 1100 // ID HSA_25816_TNFAIP8 standard; DNA; HUM; 1100 BP. XX AC 25816; XX DT 07-Sep-2005 (Created) XX DE TNFAIP8: tumor necrosis factor, alpha-induced protein 8 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 118631360..118632459 (FORWARD) CC Score Points: 6 (35.3%) CC Chromosomal Location: 5q23.1 XX CC Database Reference HGNC: 17260; TNFAIP8 CC Database Reference ENTREZGENE: 25816 CC Database Reference UNIGENE: Hs.271955 CC Database Reference ENSEMBL: ENSG00000145779 CC Database Reference REFSEQ: NM_014350 CC Database Reference REFSEQ: NP_055165 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210260_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:208296_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33243_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210260_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210260_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:208296_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:208296_x_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 118631360..118632459" FT /note="Genomic Strand: FORWARD" FT prim_transcript 927..>927 FT /db_xref="dbTSS:KDN01252" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:WMC00482" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:WMD01642" FT /note="Number of reported TSSs: 2" FT prim_transcript 1034..>1034 FT /db_xref="dbTSS:HSI04537" FT prim_transcript 1037..>1037 FT /db_xref="dbTSS:SYN08154" XX SQ Sequence 1100 BP; 234 A; 367 C; 267 G; 232 T; 0 other; gtctcccttt ccctttgtaa aacagggata gcgacaggat ctatatcata gattgttgta 60 aggagtagaa cggtgaccta cacatattaa gttttactag tattattaat atttccagcc 120 ctctgccccc cgctgccatg tactaggtgc ttaatggatg tttattgtat ggatggattc 180 atcgtactcc caccaaggtc cctcgccctt gaaaatggct accccgggcc agggctcctc 240 aacagactga aggtccagat cctactccat cctggcggtc tcgggtggcc cctgaggagg 300 gcaagccttc tgctccacag gcaaggacag tcacagctaa gtccgcgggg ggcggcagag 360 agcgagggct ttccaggagc caatgagtct ttaactccaa gaggaagccc tgcattctcc 420 gcaaatggaa accaggaatc gggagcgcgt cagctatcgt agggtagact taaggcccgc 480 agaaaattaa aagcaaaaga gcaggcggaa ttcaggggct ttcacggatc atcatcataa 540 tagtcaataa tgatggcagc agacactaac attcacgcgt tcttgttaag tgcaaggcac 600 agtgcaaatg tgtatggccc catttaacca tctcaacaca ctacgaggtt ggcgtctcat 660 ttttacaacg gaagaaactg agaggctcag gaataccgta tcctatgcac atctcccaag 720 agggtcctgt tctccagcgc ccagcgatct gggcctcgcg gtccgagtcc ggctcccggg 780 ccgccgccca gcccttctcc gcgctctcct gcgcctgggc cacttccgac tcctgctgtc 840 cggtccccag ctcctcctca cccactccgc cccgccatgc cccgccccag ccgctcggct 900 cctccttccc tgcacgctcc gcccccgacc tcccggctcc tccccggcct gcccgccaca 960 cccttggtcc ctcctgcaag ttccgcccct ggcctctgcc tccttttctc ccgccggctc 1020 taacccgcgc ttggctaagg tccgcgggaa cccgtgagcc accgagagag cagagaactc 1080 ggcgccgcca aacagcccag 1100 // ID HSA_2627_GATA6 standard; DNA; HUM; 1100 BP. XX AC 2627; XX DT 06-Sep-2005 (Created) XX DE GATA6: GATA binding protein 6 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.18 18002411..18003510 (FORWARD) CC Score Points: 2 (66.7%) CC Chromosomal Location: 18q11.1-q11.2 XX CC Database Reference HGNC: 4174; GATA6 CC Database Reference ENTREZGENE: 2627 CC Database Reference UNIGENE: Hs.514746 CC Database Reference ENSEMBL: ENSG00000141448 CC Database Reference REFSEQ: NP_005248 CC Database Reference REFSEQ: NM_005257 CC Database Reference AFFYMETRIX: AFFY_HG_U95E:80705_f_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210002_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41599_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210002_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210002_at CC Database Reference TRANSFAC GENE: G002610; GATA-6 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="18" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 18002411..18003510" FT /note="Genomic Strand: FORWARD" FT misc_feature 992 FT /note="SECONDARY ANCHOR: MMU [14465]; Alignment" FT prim_transcript 998..>998 FT /db_xref="dbTSS:HRT02462" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [14465]; Alignment" FT prim_transcript 1004..>1004 FT /db_xref="ENSEMBL:ENST00000269216" XX SQ Sequence 1100 BP; 179 A; 358 C; 335 G; 228 T; 0 other; tgccgctgac agatcggcgc tgataacccc gcgacgttca tttccagtcc cttttgcccg 60 ctagggaccg tatcagtttg tacagagttg tgataactgt ttggagggag cgaagagggg 120 gtgtgtatat gaacgtgggg gtggggaagc agcatttagc gctgggtcca gggaaggtga 180 caccccctct tcgcagtgac ttatctgtga cttacctgaa actctccagg gaaatatcag 240 aaactctcca gggacatcaa aagttggaga gcgtcctcgg acacgactga tgtggaagcc 300 cttttccatt ctgcgtaccc catagactac ctttccgtac atgacgaccc gagttaaagt 360 tcccaaaggt cagctgggga atgttgtctt gaggttcccg aaaccaccac gacctgagcc 420 gtagcatccc gagatagggt cggagaaagt ttaaggtcgg tctcacacaa cttcagggca 480 aaaagcgcat ttgctgtgaa ggggctaggc gggggttggg gggcgggggg gcgcagagca 540 cgttccccct tccttctggg ggcgtgctga cccaaggtct ggagcgcccc tcccgccgcg 600 gcggcggcgc gggactgtgc actgccaact cctcccgtgc caaggctccc tccccctccc 660 tcgtgtgggt gtgtgtgtgc gactgcggga gcgggagggt gcaccgccgc tggatgggtg 720 cgggtcgcta gccaggtcag gcgttctgtg gcctccgccc ctcccccggg gtccctgggc 780 tcggtgcccc ccgggtggac tcgcccccac tccggggaca gggcttgcgg ctcagcccac 840 gcccgcaggc agcgcggctc tcattgtctg cctgggcggc gcgctcccct cccccctcgc 900 cgtcccctcc ccaccctctt ttctctcctc ccctcgatcc ctcctcctcc tcttcacctc 960 cagcgcccag ctgctcgctg agcgcagttc cgacccacag cctggcaccc ttcggcgagc 1020 gctgtttgtt tagggctcgg tgagtccaat caggagccca ggctgcagtt ttccggcaga 1080 gcagtaagag gcgcctcctc 1100 // ID HSA_2633_1_GBP1 standard; DNA; HUM; 1100 BP. XX AC 2633_1; XX DT 05-Sep-2005 (Created) XX DE GBP1: guanylate binding protein 1, interferon-inducible, 67kDa XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 89230920..89232019 (REVERSE) CC Score Points: 2 (6.9%) CC Chromosomal Location: 1p22.2 XX CC Database Reference HGNC: 4182; GBP1 CC Database Reference ENTREZGENE: 2633 CC Database Reference UNIGENE: Hs.443527 CC Database Reference UNIGENE: Hs.62661 CC Database Reference ENSEMBL: ENSG00000117228 CC Database Reference REFSEQ: XM_375747 CC Database Reference REFSEQ: XP_375747 CC Database Reference REFSEQ: XP_375746 CC Database Reference REFSEQ: NM_002053 CC Database Reference REFSEQ: NP_002044 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202269_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:231577_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202270_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202269_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:231577_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35735_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202270_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202269_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:73236_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202270_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 89230920..89232019" FT /note="Genomic Strand: REVERSE" FT prim_transcript 998..>998 FT /db_xref="dbTSS:LFL07977" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [14469]; Alignment" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:WMC07980" XX SQ Sequence 1100 BP; 367 A; 218 C; 214 G; 301 T; 0 other; atcctggcta acacggtgaa atcccgtcac tactaaaaat acaaaaaatt tagctagatg 60 tggtggcggg cacctgtagt cccagctact caggaagctg aggcaggaga atggagtgaa 120 cccaggaggc agagcttgca gtgagctgag atcgcaccac tgcactccag cctgggcaac 180 agagcgagac tccaaaaaaa aaaatctgta tctcttgctt aataacatat gtagcaagaa 240 ctatatcctt attacttaga agaagaaaca aaggttccaa aaagaataaa taattaagtt 300 cacacagcta gtaaatatat cagagctgtc ttcatcactt agcggaatcc acaatgatta 360 tttgtttctg tgacacctac tatgaaatta gatttaagaa acctttatga gcagaaaggc 420 tcctaaccct cacacctgtg tgatactctg ctaattctga ttatttttaa tgtcctgctc 480 ccagtttgtt ttgagttgtg agctatgtgc agaaactcag tatggtcagt ctggcactca 540 gatttcttac ctgtcttctg ctacccctga caccaaggtg tggcagctta gaccaaattt 600 cctaatccat gattcataca ccttatgaga ttttgaggat actttgctta tttcggtgtt 660 atgtcatata cataataggg taaggaacat ggctgtgctt tggtcaatga taggccaaag 720 tatgacattt acgtcttgcg tgactcagag aaaattaaat aacaaatcat ttaatgtgga 780 aaccagatag aatgtttcaa tttgcctgat gctacacttt actcagcctt cgtttgtccc 840 tttttaggaa caggagcaac tactaaaaga gggatttcaa aaagaaagca gaataatgaa 900 aaatgagata caggatctcc agacgaaaat gagacgacga aaggcatgta ccataagcta 960 aagaccagag ccttcctgtc acccctaacc aaggcataat tgaaacaatt ttagaatttg 1020 gaacaagcgt cactacattt gataataatt agatcttgca tcataacacc aaaagtttat 1080 aaaggcatgt ggtacaatga 1100 // ID HSA_27289_RND1 standard; DNA; HUM; 1100 BP. XX AC 27289; XX DT 07-Sep-2005 (Created) XX DE RND1: Rho family GTPase 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.12 47545821..47546920 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 12q12-q13 XX CC Database Reference HGNC: 18314; RND1 CC Database Reference ENTREZGENE: 27289 CC Database Reference UNIGENE: Hs.124940 CC Database Reference ENSEMBL: ENSG00000172602 CC Database Reference REFSEQ: NM_014470 CC Database Reference REFSEQ: NP_055285 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210056_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37785_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210056_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210056_at CC Database Reference TRANSFAC GENE: G005410; RHO6 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="12" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 47545821..47546920" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000309739" XX SQ Sequence 1100 BP; 330 A; 266 C; 274 G; 230 T; 0 other; gaggccaagg cgggcggatc gcctgaggtc gggagttcga gaccagcctg accaacatgg 60 agaaaccccg tctctactaa aaatacaaca ttagctgggc atggtggtgc atgcctgtaa 120 tcccagctac tcgggaggct gaggcaggag aatcgcttga atccgggaga tggaggttgc 180 agtgagctga gatcgtgcca ttgcactcca gcctgggcaa caagagcgaa actccatctc 240 aaaataaata aataaataaa taaataaata aataaataaa taaataaata aataaaagag 300 gtacagcagg agctgatatt gggaggggaa ataaagggaa gtaagaactg gtttggatgg 360 gaattagaaa aaacaaaaaa gtcagacatc aggccaggcg ctgtggctca tgtctgtagt 420 cccagcactt tgggaggctg agacaggcgg attgcttgag cccagaagtt caagaccagc 480 ctggataaca tggtgagacc cctgtctcta tttaaaacaa aagatgtaag gaaaaaaaag 540 aaaaaaaatg tcagagaagt tctgggccac ctcccccatc ccctactcct ccaaaacaca 600 cacacacaca cacacctgtc tatagtctaa gcaggtcctg cttttgtaac ccacccggga 660 cagtccctgc aactccagcc tgacctcact tcctgcttcc atagctagtt tgtttttctg 720 acacttattg gtagacactc cagatcattt cattttgctt ccagtaccct ttccacttcc 780 taatacaaat gcaaaacaac ctgggaatcc cctttcaggg ggaaacaacg gtgcagcttt 840 aagagaaaga gaagggagga agggggcgct gactcagatc ctcagatcca ttggctgctg 900 gagggaatcc cacctcaggg attgggcgta acagagtccg cctcctcttg tgattggctc 960 agccagaaaa ataaaaggcg gctgtgccgg cctcctcctc agttggaggg aggcagggaa 1020 tctggcttga ttggcgtgct gagacgcacc tggcgcaacc ctcccttctg aatcgaagtt 1080 caagtcccgc ggacactgca 1100 // ID HSA_2920_CXCL2 standard; DNA; HUM; 1100 BP. XX AC 2920; XX DT 06-Sep-2005 (Created) XX DE CXCL2: chemokine (C-X-C motif) ligand 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 75329848..75330947 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 4q21 XX CC Database Reference HGNC: 4603; CXCL2 CC Database Reference ENTREZGENE: 2920 CC Database Reference UNIGENE: Hs.75765 CC Database Reference ENSEMBL: ENSG00000081041 CC Database Reference REFSEQ: NP_002080 CC Database Reference REFSEQ: NM_002089 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209774_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209774_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209774_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37187_at CC Database Reference TRANSFAC GENE: G000280; GRO2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 75329848..75330947" FT /note="Genomic Strand: REVERSE" FT misc_signal 920..935 FT /note="TRANSFAC Site R03341" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000264492" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: HSA [2919]; Alignment" XX SQ Sequence 1100 BP; 289 A; 330 C; 253 G; 228 T; 0 other; gcaatctagt atgtatatat cagacatgtc tgcttgtgct tagagtagta aacaagcgga 60 gtctcattcc ctgctccttt tctggtggtg tctatggcct tttctgccca gggacagcac 120 tagaaaaggc agacctcctg agcccaacag gcccctcgca gctcccagtg acttccatgg 180 atcaaaacac agacttccat acaacaaaaa attgatgcta ctggaattac tagagttcga 240 gatgttccaa gatttcaaag agagaaagga tgggggattg caacactgtt aactaaaata 300 aacactgaat tgacccttgg caatggtctg ttcccgcacc caacacctgg ctccactacg 360 ttgaaacaca cacacacaca cacacacaca cacacacaca cacacacaca cgtgatattt 420 gcttttaaga tcataaaaca ccaggaagga gacaaaagct cttatgcgtc atctgagatg 480 acacatgtac tgttaaagcg tgcgtttatt tcaaacatta atgaaatttg cagaacccaa 540 actaaagaga gaggatagat aagacatgct gcagttcttg ccctaacttt caatcccaac 600 aactgaaatg tcttccagag aagtaactcc ccccggtaag gatgtagcgc ggtccctacg 660 tgggtctaag ggatctgacc cacgacgcac tgcactgggt tcacgaagcg cctcctcgca 720 ggcggttatc tcggtatctc tgagagcggc gggctctcgc tcccgctcca gggattcggg 780 gcagaaagag aacatcccac agttggcggg agttacgcaa gacagtcaga cccggacgtc 840 actcgtgagt gccccgaccc ccctccaccc cagaggcggg gccatcgcct tccttccgaa 900 ctcgggatcg atctggagct ccgggaattt ccctggcccg ggactccggg ctttccagcc 960 ccaaccatgc ataaaagggg ttcgccgttc tcggagagcc acagagcccg ggccacaggc 1020 agctccttgc cagctctcct cctcgcacag ccgctcgaac cgcctgctga gccccatggc 1080 ccgcgccacg ctctccgccg 1100 // ID HSA_2921_CXCL3 standard; DNA; HUM; 1100 BP. XX AC 2921; XX DT 06-Sep-2005 (Created) XX DE CXCL3: chemokine (C-X-C motif) ligand 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 75269342..75270441 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 4q21 XX CC Database Reference HGNC: 4604; CXCL3 CC Database Reference ENTREZGENE: 2921 CC Database Reference UNIGENE: Hs.89690 CC Database Reference ENSEMBL: ENSG00000163734 CC Database Reference REFSEQ: NP_002081 CC Database Reference REFSEQ: NM_002090 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207850_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34022_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207850_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207850_at CC Database Reference TRANSFAC GENE: G000281; GRO3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 75269342..75270441" FT /note="Genomic Strand: REVERSE" FT misc_feature 265..971 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF6_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF6_panc" FT /note="PubMed:14988562" FT misc_signal 919..934 FT /note="TRANSFAC Site R03342" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000296026" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: HSA [2919]; Alignment" FT /note="PRIMARY ANCHOR: MMU [14825]; Alignment" XX SQ Sequence 1100 BP; 278 A; 312 C; 278 G; 232 T; 0 other; cttcagtggg aatggtgttt gcacaccagg tacctactct ctagtgtcat tcgcaaagac 60 agaaccagaa acattgagcc catgatcctg ctggacccag cccctccaca gcttcagagt 120 gacagccagt gtcatatttc tagatcaaat ctgaatccct cccactggga gaaggtctcc 180 aggggattta ggaagttcca acatttcaga gggaggaagg acgttatgca ggatacaaaa 240 gaagaggtca tgttatacag ccctggcttc cacggacact aacactgaat tcaaattttg 300 acactgataa tctgttgcca ccaaatggaa aacgtaaaca aggtattcta agtgtgatta 360 gagaatatgc aaaacaagga acaagtagaa cattcttctc tggaatccga gacgatggct 420 gtactttcac agagagcatg atgttagatg tacatgaaat aacgctaaac cgaaaatgag 480 agaggcagag accgggaggt taacatagag gatagactat atagagagag gatagctgag 540 ggaaaactcg cctgtctccg ggtccccagc aaatctgata actaaggaga caaagctctc 600 ttcctctaaa gaagtcgtgc ctttcctgtc ctggttctca cgggtccccc cagctctttc 660 ctccaaccct accccgtacg cggggggtca tcggggacct aaggtccccc ctcacaggct 720 gtatcttcag cgaggtggac tcactgcctc tccaggaatt tggggcagaa aatgaatatc 780 ccaaagtccc agagtgcacg ggggttactc tggagggcga ggcgtaggcg tcaccagtgg 840 gctcccccta cccgtatccg actccacccc gggggcgggg ccgtcgcctt ccttcgggac 900 tccggatcga tctggagctc cgggaatttc cctggcccgg ccgctccggg ctttccagtc 960 tcaaccatgc ataaaaaggg ttcgccgatc ttggggagcc acacagcccg ggtcgcaggc 1020 acctccccgc cagctctccc gcttctcgca cagcttcccg acgcgtctgc tgagccccat 1080 ggcccacgcc acgctctccg 1100 // ID HSA_3097_HIVEP2 standard; DNA; HUM; 1100 BP. XX AC 3097; XX DT 06-Sep-2005 (Created) XX DE HIVEP2: human immunodeficiency virus type I enhancer binding protein DE 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 143137399..143138498 (REVERSE) CC Score Points: 3 (20.0%) CC Chromosomal Location: 6q23-q24 XX CC Database Reference HGNC: 4921; HIVEP2 CC Database Reference ENTREZGENE: 3097 CC Database Reference UNIGENE: Hs.510172 CC Database Reference ENSEMBL: ENSG00000010818 CC Database Reference REFSEQ: NM_006734 CC Database Reference REFSEQ: NP_006725 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212641_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212642_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212641_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212641_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212642_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212642_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36175_s_at CC Database Reference TRANSFAC GENE: G013850; HIVEP2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 143137399..143138498" FT /note="Genomic Strand: REVERSE" FT prim_transcript 824..>824 FT /db_xref="ENSEMBL:ENST00000012134" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [15273]; Alignment" FT prim_transcript 1075..>1075 FT /db_xref="dbTSS:OFR05291" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 338 A; 196 C; 217 G; 349 T; 0 other; gagacggggt ttcaccattt tggccaggat ggtttcagtc tcttgacctc gtgatccacc 60 tgcctcagcc tccccaaatg ctgggtttac aggcgtgagc caccatgcct ggccacatat 120 tgtttgtatt aagctataaa acatatctct atatagagat atgtaataca ctttggcata 180 caagtcataa aacttggtta ggaatagctc tatttttttt taatggggct ttctaaaacc 240 ttatactttt gtagataata tccatcaagg attttccttc aaatggtttt ctaaagttaa 300 aaagtattta aaagagtgac caaaattcaa acatggaaga gacttatgtt catgacttaa 360 tgctgagttt gaaattaata tattttaatt gtggaattaa tgtaatctca ataaaaataa 420 ttccttggag taaaaaacat ttcaaattta tctaatttct ggttggttag ttaggttttt 480 tttttttttg gtttcttatt tgaaactgtt atgacaatct ctttgtattt tctttttctt 540 cagatcattt tatcttagtg aaactggcaa ttgaactttg ctctagttga tgggcaaaat 600 ttctcctaga ctattcatca tcccaatttc atcctagttg aaaattttca aatgccataa 660 gaaatcttta tagatttgca cttagctttt ggatggacgt ttctacaatg gagagaactg 720 tgttatagcc ctggtccaag gacattacta gctaatgccc atcgactgtg gtgtgcgtgt 780 ggaaggttcc aaagagaagg agcaatcagc aagtttgcag acaccctgga acatggaagc 840 aaccaagctt taagaagcac agctttggag acactccatg agtctgcact gctttcaggg 900 gaactagcac ttaagacctt gtgtaacaaa atggacactg gggacacagc tctaggacaa 960 aaagctacct caaggtctgg agaaactgat aaagcatcag gtagatggag acaggaacaa 1020 tcagctgtta ttaagatgag cacttttggc agtcatgaag gacagcggca accacaaata 1080 gagcctgagc aaatcggaaa 1100 // ID HSA_330_BIRC3 standard; DNA; HUM; 1100 BP. XX AC 330; XX DT 06-Sep-2005 (Created) XX DE BIRC3: baculoviral IAP repeat-containing 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.11 101692404..101693503 (FORWARD) CC Score Points: 2 (22.2%) CC Chromosomal Location: 11q22 XX CC Database Reference HGNC: 591; BIRC3 CC Database Reference ENTREZGENE: 330 CC Database Reference UNIGENE: Hs.127799 CC Database Reference ENSEMBL: ENSG00000023445 CC Database Reference REFSEQ: NP_001156 CC Database Reference REFSEQ: NM_001165 CC Database Reference REFSEQ: NM_182962 CC Database Reference REFSEQ: NP_892007 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210538_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:88714_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:91017_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:230499_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210538_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1717_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210538_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:63769_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:230499_at CC Database Reference TRANSFAC GENE: G004064; c-IAP2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="11" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 101692404..101693503" FT /note="Genomic Strand: FORWARD" FT misc_feature 887 FT /note="SECONDARY ANCHOR: MMU [11796]; Alignment" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000263464" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 330 A; 225 C; 248 G; 297 T; 0 other; ctcagctcag tccaattgcg tgcagaatgc actggatgct gtttccacag aacgatgaag 60 tctccaataa tctttatggg ctctgtctct ggttggtaat tgtctttgat ctactggaag 120 atagaaaatc agatgagctc tccaaatcca tctgttaccc tggtacggat ggctctcaga 180 taaagttgct taaatttact gcttagagaa cgttgaggga aatatggcag tgcaattaga 240 ctcaaagatg tcaggtttcc ctgagaatgg cactgcaact cagaaacctg ccctgtgaga 300 tcaaaggcta taaaggaggg atttttttaa gtagccaact ccaccctact tattaaaaaa 360 aaaaaaaaaa caactcacca aaccaaacaa aagtatttcc atacagaaaa tttaccaagc 420 catttcaatc tttaaaatgg taaaataaac tgcaaaggag aactgcatga tttttttcac 480 atacccctac atttcctttc acctcttact ttcttgatca gaacaaaaag taaaaataaa 540 tagaaatatt tcacaaagtt tcgatttttt tttttttaaa tgctggactt ctgcagctat 600 agtagaagat tgaaaaacct aaccttttta cgtgtaaagt gtatggcgga tggagggtgg 660 agaacagggc atattgacct tttccaggca ggctaagcaa tgatcgtcct ctctatatgg 720 gttgttatca agatttcctc tgacccacga gcaatgaagc aaatgtcttt cagtaaatgc 780 cgcgaagata tgccacggtt aagagtcatg cttttgggtc atggaaatcc ccgagtgggt 840 ttgccaggcc actgattaag aggaagtgtg tgtggttatt accgctggag ttcccctaag 900 tcctaaaagg aaagcaccag tgcacatgca aaccactggg aggagtgcgg aacgcctggt 960 acagataggg gtggggattt gggtgacgca tttaaaagac agcgtgagac tcgcgccctc 1020 cggcacggaa aaggccaggc gacaggtgtc gcttgaaaag actgggcttg tccttgctgg 1080 tgcatgcgtc gtcggcctct 1100 // ID HSA_3383_ICAM1 standard; DNA; HUM; 1100 BP. XX AC 3383; XX DT 05-Sep-2005 (Created) XX DE ICAM1: intercellular adhesion molecule 1 (CD54), human rhinovirus DE receptor XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.19 10241789..10242888 (FORWARD) CC Score Points: 97 (89.8%) CC Chromosomal Location: 19p13.3-p13.2 XX CC Database Reference HGNC: 5344; ICAM1 CC Database Reference ENTREZGENE: 3383 CC Database Reference UNIGENE: Hs.515126 CC Database Reference ENSEMBL: ENSG00000090339 CC Database Reference REFSEQ: NM_000201 CC Database Reference REFSEQ: NP_000192 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202638_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207194_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:215485_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:215485_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202637_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35078_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202638_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32640_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:215485_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207194_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202637_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207194_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202638_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202637_s_at CC Database Reference TRANSFAC GENE: G001071; ICAM-1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="19" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 10241789..10242888" FT /note="Genomic Strand: FORWARD" FT prim_transcript 729..>729 FT /db_xref="dbTSS:SYN09326" FT misc_signal 805..822 FT /note="TRANSFAC Site R08087" FT misc_signal 817..837 FT /note="TRANSFAC Site R08088" FT /note="TRANSFAC Site R13475" FT prim_transcript 882..>882 FT /db_xref="dbTSS:LFL02065" FT prim_transcript 902..>902 FT /db_xref="dbTSS:LFL09295" FT /note="Number of reported TSSs: 3" FT prim_transcript 970..>970 FT /db_xref="dbTSS:T3R05169" FT prim_transcript 977..>977 FT /db_xref="ENSEMBL:ENST00000264832" FT prim_transcript 998..>998 FT /db_xref="dbTSS:SPL05195" FT /note="Number of reported TSSs: 5" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [15894]; Alignment" FT /note="PRIMARY ANCHOR: RNO [25464]; Alignment" FT prim_transcript 1005..>1005 FT /db_xref="dbTSS:MPG01568" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:CAS10961" FT /note="Number of reported TSSs: 2" FT prim_transcript 1008..>1008 FT /db_xref="EPD:EP73783" FT misc_feature 1008 FT /note="PRIMARY ANCHOR: MMU [15894]; Alignment" FT /note="PRIMARY ANCHOR: RNO [25464]; Alignment" FT prim_transcript 1009..>1009 FT /db_xref="dbTSS:LFL03104" FT /note="Number of reported TSSs: 3" FT prim_transcript 1028..>1028 FT /db_xref="dbTSS:LFL05106" FT misc_feature 1046 FT /note="SECONDARY ANCHOR: RNO [25464]; Alignment" FT misc_feature 1048 FT /note="SECONDARY ANCHOR: MMU [15894]; Alignment" XX SQ Sequence 1100 BP; 189 A; 345 C; 360 G; 206 T; 0 other; tttagtgcat gagcctgggt tcgagttgcc ggagcctcgc gcgtagggca ggggttcgag 60 cgccccttct ccctgcctcg cctctgcgcc tgggggctgc tgcctcagtt tcccagcgac 120 aggcagggat ttcgagcgtc cccctcccct ccctcgtcaa gatccaagct agctgcctca 180 gtttccccgc ggagcctggg acgccagcgg aggggctcgg cgcgtaggga tcacgcagct 240 tccttccttt ttctgggagc tgtaaagacg cctccgcggc caaggccgaa aggggaagcg 300 aggaggccgc cggggtgagt gccctcgggt gtagagagag gacgccgatt tccccggacg 360 tggtgagacc gcgcttcgtc actcccacgg ttagcggtcg ccgggaggtg cctggctctg 420 ctctggccgc ttctcgagaa atgcccgtgt cagctaggtg tggacgtgac ctagggggag 480 gggcatccct cagtggaggg agcccgggga ggattcctgg gcccccaccc aggcaggggg 540 ctcatccact cgattaaaga ggcctgcgta agctggagag ggaggacttg agttcggacc 600 ccctcgcagc ctggagtctc agtttaccgc tttgtgaaat ggacacaata acagtctcca 660 ctctccgggg aagttggcag tatttaaaag tacttaataa accgcttagc gcggtgtaga 720 ccgtgattca agcttagcct ggccgggaaa cgggaggcgt ggaggccggg agcagccccc 780 ggggtcatcg ccctgccacc gccgcccgat tgctttagct tggaaattcc ggagctgaag 840 cggccagcga gggaggatga ccctctcggc ccgggcaccc tgtcagtccg gaaataactg 900 cagcatttgt tccggagggg aaggcgcgag gtttccggga aagcagcacc gccccttggc 960 ccccaggtgg ctagcgctat aaaggatcac gcgccccagt cgacgctgag ctcctctgct 1020 actcagagtt gcaacctcag cctcgctatg gctcccagca gcccccggcc cgcgctgccc 1080 gcactcctgg tcctgctcgg 1100 // ID HSA_3459_IFNGR1 standard; DNA; HUM; 1100 BP. XX AC 3459; XX DT 05-Sep-2005 (Created) XX DE IFNGR1: interferon gamma receptor 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 137582096..137583195 (REVERSE) CC Score Points: 85 (93.4%) CC Chromosomal Location: 6q23-q24 XX CC Database Reference HGNC: 5439; IFNGR1 CC Database Reference ENTREZGENE: 3459 CC Database Reference UNIGENE: Hs.520414 CC Database Reference ENSEMBL: ENSG00000027697 CC Database Reference REFSEQ: NP_000407 CC Database Reference REFSEQ: NM_000416 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211676_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202727_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202727_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211676_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1038_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211676_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202727_s_at CC Database Reference TRANSFAC GENE: G003410; IFNGR1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 137582096..137583195" FT /note="Genomic Strand: REVERSE" FT misc_feature 322..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT prim_transcript 954..>954 FT /db_xref="dbTSS:HEP14391" FT prim_transcript 957..>957 FT /db_xref="ENSEMBL:ENST00000029439" FT /db_xref="dbTSS:COL09438" FT /note="Number of reported TSSs: 2" FT prim_transcript 960..>960 FT /db_xref="dbTSS:HRT03726" FT /note="Number of reported TSSs: 5" FT prim_transcript 962..>962 FT /db_xref="dbTSS:HEP00115" FT /note="Number of reported TSSs: 5" FT prim_transcript 979..>979 FT /db_xref="dbTSS:SZR04365" FT prim_transcript 980..>980 FT /db_xref="dbTSS:HRT02133" FT prim_transcript 981..>981 FT /db_xref="dbTSS:LNG12834" FT /note="Number of reported TSSs: 5" FT prim_transcript 984..>984 FT /db_xref="dbTSS:LNF02227" FT prim_transcript 998..>998 FT /db_xref="dbTSS:SYN09040" FT /note="Number of reported TSSs: 2" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:MPB06521" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:LNG11516" FT /note="Number of reported TSSs: 2" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:HRT03881" FT prim_transcript 1008..>1008 FT /db_xref="EPD:EP74074" FT prim_transcript 1011..>1011 FT /db_xref="dbTSS:SYN02201" FT /note="Number of reported TSSs: 2" FT prim_transcript 1020..>1020 FT /db_xref="dbTSS:SYN08016" FT /note="Number of reported TSSs: 2" FT prim_transcript 1052..>1052 FT /db_xref="dbTSS:HRT04864" FT prim_transcript 1099..>1099 FT /db_xref="dbTSS:LNG12952" XX SQ Sequence 1100 BP; 317 A; 246 C; 283 G; 254 T; 0 other; tatagtgtct ttataaggat tttccctctt taaaaatttt ccttaacact agtaatcatg 60 cagtctttca ctcaacaaat actaattgag tgccaagtaa agatgtcagc tctacggagc 120 ttacatttta gaaggagaag aaaacaaata tcaaggtgta tattatagtg tacagcaagg 180 tgaaaagtgc catgaaaaaa cagtagggcg gggtaaggag gaggagaagg tgtgttgcaa 240 tttaaaattt ttaacaaaag ttcatgatac tcagagaatt gaaacaggtg agatcattag 300 acattcgcat gtttgagcac aagcgctgaa ggacttagca atgtggctgc agtggaatag 360 gagagatgca aaataacaga caaacccaga gaggtaagag agcagacctc ttcatgagag 420 gctgcctgat aaactgattt gacactgaat tgctgagaag gtaatgcaaa tagttttttt 480 ctccaagaac aaagtagttc ttggtcaagc cgatttgatt tgggctgtgg gaatctgcac 540 aaaccatttc actagctaag tctcaggttc ctcaaatgaa aaagcaggga ctggaaatgg 600 cttttgaagt ctcattctct tctaaaaatg tcaggctcca agacaaccag gtgaagtcca 660 agagttagta aaataaggat tgtggctcgg ctgtggccta atgcaaactt gcacaacccc 720 aggaaaccga aaaaaactgg aagaagaatt gcagaatggg gtgccaggtt gaaagacctt 780 aacctttgca ctcaaattcc tcccacaccc agaagtccag gtcccgaccg cacgacgccg 840 tgctcactgc tgggtgctgc gcctgagtcc gcctcctgcg gcttcccgga cttgaccccg 900 cccacgccct ggtcccgcct cctgccgacg ccggcacaga ccccggtgac ggaagtgacg 960 taaggccggg gctggagggc agtgctgggc tggtcccgca ggcgctcggg gttggagcca 1020 gcgaccgtcg gtagcagcat ggctctcctc tttctcctac cccttgtcat gcagggtgtg 1080 agcagggctg agatgggcac 1100 // ID HSA_3552_IL1A standard; DNA; HUM; 1100 BP. XX AC 3552; XX DT 06-Sep-2005 (Created) XX DE IL1A: interleukin 1, alpha XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 113258202..113259301 (REVERSE) CC Score Points: 56 (98.2%) CC Chromosomal Location: 2q14 XX CC Database Reference HGNC: 5991; IL1A CC Database Reference ENTREZGENE: 3552 CC Database Reference UNIGENE: Hs.1722 CC Database Reference ENSEMBL: ENSG00000115008 CC Database Reference REFSEQ: NP_000566 CC Database Reference REFSEQ: NM_000575 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210118_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210118_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210118_s_at CC Database Reference TRANSFAC GENE: G003389; IL1A XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="2" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 113258202..113259301" FT /note="Genomic Strand: REVERSE" FT prim_transcript 100..>100 FT /db_xref="ENSEMBL:ENST00000263339" FT prim_transcript 995..>995 FT /db_xref="dbTSS:SMR08628" FT /note="Number of reported TSSs: 2" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP14063" XX SQ Sequence 1100 BP; 320 A; 279 C; 190 G; 311 T; 0 other; gaacccaaaa cattcatttg ctaagagtct ggtgttctac cacctgaact aggctggcca 60 caggaattat aaaagctgag aaattcttta ataatagtaa ccaggcaaca ccattgaagg 120 ctcatatgta aaaatccatg ccttcctttc tcccaatctc cattcccaaa cttagccact 180 ggcttctggc tgaggcctta cgcatacctc ccggggcttg cacacacctt cttctacaga 240 agacacacct tgggcatatc ctacagaaga ccaggcttct ctctggtcct tggtagaggg 300 ctactttact gtaacagggc cagggtggag agttctctcc tgaagctcca tcccctctat 360 aggaaatgtg ttgacaatat tcagaagagt aagaggatca agacttcttt gtgctcaaat 420 accactgttc tcttctctac cctgccctaa ccaggagctt gtcaccccaa actctgaggt 480 gatttatgcc ttaatcaagc aaacttccct cttcagaaaa gatggctcat tttccctcaa 540 aagttgccag gagctgccaa gtattctgcc aattcaccct ggagcacaat caacaaattc 600 agccagaaca caactacagc tactattaga actattatta ttaataaatt cctctccaaa 660 tctagcccct tgacttcgga tttcacgatt tctcccttcc tcctagaaac ttgataagtt 720 tcccgcgctt ccctttttct aagactacat gtttgtcatc ttataaagca aaggggtgaa 780 taaatgaacc aaatcaataa cttctggaat atctgcaaac aacaataata tcagctatgc 840 catctttcac tattttagcc agtatcgagt tgaatgaaca tagaaaaata caaaactgaa 900 ttcttccctg taaattcccc gttttgacga cgcacttgta gccacgtagc cacgcctact 960 taagacaatt acaaaaggcg aagaagactg actcaggctt aagctgccag ccagagaggg 1020 agtcatttca ttggcgtttg agtcagcaaa ggtattgtcc tcacatctct ggctattaaa 1080 gtattttctg ttgttgtttt 1100 // ID HSA_3554_1_IL1R1 standard; DNA; HUM; 1100 BP. XX AC 3554_1; XX DT 06-Sep-2005 (Created) XX DE IL1R1: interleukin 1 receptor, type I XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 102178633..102179732 (FORWARD) CC Score Points: 3 (14.3%) CC Chromosomal Location: 2q12 XX CC Database Reference HGNC: 5993; IL1R1 CC Database Reference ENTREZGENE: 3554 CC Database Reference UNIGENE: Hs.551050 CC Database Reference UNIGENE: Hs.516249 CC Database Reference ENSEMBL: ENSG00000115594 CC Database Reference REFSEQ: NM_000877 CC Database Reference REFSEQ: NP_000868 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:215561_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202948_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:215561_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202948_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1368_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202948_at CC Database Reference TRANSFAC GENE: G003129; IL1R1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="2" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 102178633..102179732" FT /note="Genomic Strand: FORWARD" FT prim_transcript 920..>920 FT /db_xref="dbTSS:HCR04105" FT prim_transcript 984..>984 FT /db_xref="dbTSS:LFL07409" XX SQ Sequence 1100 BP; 287 A; 255 C; 321 G; 237 T; 0 other; gagaatgttc atcggagtgc agagcacagg aggagctatg agagaaataa aagaggcagg 60 ccaggtgcgg tggctcatgc ctgtaacccc agcactttgg gaggccaagg gggtggatca 120 tctgagttca ggagtttgag accagcctga ccatcatggt gaaaccccat ctctactaaa 180 attacaaaaa ttagccagac atggtggcgg gcatctataa tcccagctac tcgggctgag 240 gcacgagaat cacttgaacc tgggaagcag gggttgctgt gagccgagat tgtgacattg 300 cactccagcc tgggagacag agcaagactg tctcagaaaa aaaaaaaaaa aaaaaaaaga 360 ggaggcttgg cagcaccagc tctcctaggt ggatctggct gcatttgtgg aagccagagg 420 ctccagcttt catctccctg agctgagggg tgatcagtgg ccatcccacc tccagggtgt 480 ggtgaaggga gacttccaga gttctcaggg cacatggcag gagtggtggc caccatgaga 540 agtgggccag catctgggac acgagcagac ctgaataaag agtcctgcag cattgcctgg 600 gctgactcta gggagattgc tctaaggatt gggaggtagg cagagaggga aagcttaggc 660 caccacaggc ctgagactga ccagtcaaga ctctgatgat gggaacatga taatgagctg 720 gattcagcca gcaggcttgt ccaggttcaa cacaaagtca tgagaggaaa gcaccagctt 780 cgggaaactt tagaggttac cgtgcagtgg cgggtgttgg tgtttcttaa gggtctggca 840 cgtttgctga gtgattctgg ctgtctgcct ggctctgagc ttcctgttca tagttcccca 900 gatgtgtcac ggccgaggga ttaaagccct aagaggctgt gacacagcca tctccaaaac 960 cccactttct ccttcctttg agcctccgta ccagctgggg cgtccggcaa gatgtgagtt 1020 gtcactctgc tgcggcacag acctgaatta acaactctag ctagggctga cttcaaaaag 1080 cactttcgtt ttttaataac 1100 // ID HSA_3575_IL7R standard; DNA; HUM; 1100 BP. XX AC 3575; XX DT 06-Sep-2005 (Created) XX DE IL7R: interleukin 7 receptor XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 35891753..35892852 (FORWARD) CC Score Points: 2 (66.7%) CC Chromosomal Location: 5p13 XX CC Database Reference HGNC: 6024; IL7R CC Database Reference ENTREZGENE: 3575 CC Database Reference UNIGENE: Hs.362807 CC Database Reference ENSEMBL: ENSG00000168685 CC Database Reference REFSEQ: NP_002176 CC Database Reference REFSEQ: NM_002185 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205798_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36227_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205798_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1370_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:63628_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205798_at CC Database Reference TRANSFAC GENE: G003198; IL7R XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 35891753..35892852" FT /note="Genomic Strand: FORWARD" FT misc_feature 970 FT /note="SECONDARY ANCHOR: MMU [16197]; Alignment" FT prim_transcript 996..>996 FT /db_xref="ENSEMBL:ENST00000303115" FT prim_transcript 1005..>1005 FT /db_xref="ENSEMBL:ENST00000343305" XX SQ Sequence 1100 BP; 328 A; 233 C; 221 G; 318 T; 0 other; gaggctgtat tccaatgaaa cgttatttgc aaaaacaggt ggtagattaa atttggtccc 60 aaggcttact tgggaaaaaa aaagatcttt tgaaaaagaa aaaataaatg aataattttt 120 taaaaaattg ttccctaggt catagtttgc cagcccctgc cctaaacaaa taattcttga 180 atgcctactg tggtgtgtaa gatatgagta aataccaggg atacacagag aacaaaagag 240 aaaaactgct attcttgtga aacttggaag ttggaggtaa gctatttaaa ataaacccac 300 aataaagtac ttcacatagt gcagactgtt tctttaaatc aaaactcact ccaaacaacc 360 aattgattca ctttgtaagt ttgaattttt gtcttcagat tcttttaaag tgggccctta 420 gtcaggagcg gtggctcatg cctgtagtcc tagcactttg ggaggctgag gcaggcagat 480 cacttgaggt caggagttcg agacaagcct ggccaacatg gcgaaacccc gtctccactg 540 aaaacacaaa aattaggctg gcatagtggc atttgcctgt agtcctagct actcaggagg 600 ctgaggcagg agaattgctt gaacctggga ggtggaaatt gcagtgagcc gagatcatgc 660 tattgtactc cagcctgggc aacaaagcaa gactctgtct caaaaaaata aaaattaaaa 720 aaataaagta gcctctagcc taagatagct tgagcctagg tgtgaatcta ctgccttact 780 ctgatgtaag cacagtaagt gtgggggctg cagggaatat ccaggaggaa caataatttc 840 agaggctctg tctcttcatg tccttgacct ctgcttacag cagcaatact tttactcaga 900 cttcctgttt ctggaacttg ccttcttttt tgctgtgttt atacttccct tgtctgtggt 960 tagataagta taaagcccta gatctaagct tctctgtctt cctccctccc tcccttcctc 1020 ttactctcat tcatttcata cacactggct cacacatcta ctctctctct ctatctctct 1080 cagaatgaca attctaggta 1100 // ID HSA_3576_1_IL8 standard; DNA; HUM; 1100 BP. XX AC 3576_1; XX DT 05-Sep-2005 (Created) XX DE IL8: interleukin 8 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 74970321..74971420 (FORWARD) CC Score Points: 69 (93.2%) CC Chromosomal Location: 4q13-q21 XX CC Database Reference HGNC: 6025; IL8 CC Database Reference ENTREZGENE: 3576 CC Database Reference UNIGENE: Hs.624 CC Database Reference ENSEMBL: ENSG00000169429 CC Database Reference REFSEQ: NM_000584 CC Database Reference REFSEQ: NP_000575 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202859_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211506_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1369_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211506_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202859_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211506_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35372_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202859_x_at CC Database Reference TRANSFAC GENE: G000317; IL8 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 74970321..74971420" FT /note="Genomic Strand: FORWARD" FT misc_signal 82..94 FT /note="TRANSFAC Site R05060" FT misc_signal 896..909 FT /note="TRANSFAC Site R02908" FT misc_signal 910..919 FT /note="TRANSFAC Site R02909" FT prim_transcript 990..>990 FT /db_xref="ENSEMBL:ENST00000307407" FT prim_transcript 997..>997 FT /db_xref="dbTSS:CAS01565" FT prim_transcript 999..>999 FT /db_xref="dbTSS:CAS11042" FT /note="Number of reported TSSs: 4" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:CAS08864" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP73083" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:Sm+A0070.seq" FT prim_transcript 1029..>1029 FT /db_xref="dbTSS:CAS05087" XX SQ Sequence 1100 BP; 351 A; 244 C; 174 G; 331 T; 0 other; tttccactaa gcatacaact ttccattaga taacacctcc ctcccacccc aaccaagcag 60 ctccagtgca ccactttctg gagcataaac ataccttaac tttacaactt gagtggcctt 120 gaatactgtt cctatctgga atgtgctgtt ctctttcatc ttcctctatt gaagccctcc 180 tattcctcaa tgccttgctc caactgcctt tggaagattc tgctcttatg cctccactgg 240 aattaatgtc ttagtaccac ttgtctattc tgctatatag tcagtcctta cattgctttc 300 ttcttctgat agaccaaact ctttaaggac aagtacctag tcttatctat ttctagatcc 360 cccacattac tcagaaagtt actccataaa tgtttgtgga actgatttct atgtgaagca 420 catgtgcccc ttcactctgt taacatgcat tagaaaacta aatcttttga aaagttgtag 480 tatgccccct aagagcagta acagttccta gaaactctct aaaatgctta gaaaaagatt 540 tattttaaat tacctcccca ataaaatgat tggctggctt atcttcacca tcatgatagc 600 atctgtaatt aactgaaaaa aaataattat gccattaaaa gaaaatcatc catgatcttg 660 ttctaacacc tgccactcta gtactatatc tgtcacatgg tactatgata aagttatcta 720 gaaataaaaa agcatacaat tgataattca ccaaattgtg gagcttcagt attttaaatg 780 tatattaaaa ttaaattatt ttaaagatca aagaaaactt tcgtcatact ccgtatttga 840 taaggaacaa ataggaagtg tgatgactca ggtttgccct gaggggatgg gccatcagtt 900 gcaaatcgtg gaatttcctc tgacataatg aaaagatgag ggtgcataag ttctctagta 960 gggtgatgat ataaaaagcc accggagcac tccataaggc acaaactttc agagacagca 1020 gagcacacaa gcttctagga caagagccag gaagaaacca ccggaaggaa ccatctcact 1080 gtgtgtaaac atgacttcca 1100 // ID HSA_3600_IL15 standard; DNA; HUM; 1100 BP. XX AC 3600; XX DT 06-Sep-2005 (Created) XX DE IL15: interleukin 15 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 142914359..142915458 (FORWARD) CC Score Points: 1 (50.0%) CC Chromosomal Location: 4q31 XX CC Database Reference HGNC: 5977; IL15 CC Database Reference ENTREZGENE: 3600 CC Database Reference UNIGENE: Hs.311958 CC Database Reference ENSEMBL: ENSG00000164136 CC Database Reference REFSEQ: NM_172174 CC Database Reference REFSEQ: NP_751915 CC Database Reference REFSEQ: NP_751914 CC Database Reference REFSEQ: NM_172175 CC Database Reference REFSEQ: NP_000576 CC Database Reference REFSEQ: NM_000585 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205992_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205992_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:217371_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205992_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:217371_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:217371_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:66883_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38488_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1036_at CC Database Reference TRANSFAC GENE: G006283; IL15 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 142914359..142915458" FT /note="Genomic Strand: FORWARD" FT misc_feature 428..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000296545" XX SQ Sequence 1100 BP; 250 A; 305 C; 261 G; 284 T; 0 other; tttttcataa aaatatgaaa ttatattata cggaacttta tgtacatgga aagtgaataa 60 tttctattat ttttctattt gatatttatc atatttatgt aattaaaaac ataattaaat 120 tttaaactaa attaaactgc gctccaggaa gacatcattt tctctgaacc atgactctga 180 aaatttggaa agcaccgtac aagagggatt ttcagtgatt cacaagagtg caagattctg 240 caaagtactt tcaaaactaa gcgtgagatc tttgctactg cctttatggc atgcaaatca 300 ctcagcctca actcagttcc ttcctccaat gtaaaaatac tacaagaaca acatctcacg 360 cttccatcaa atgggaccat gtgtgatatt ttacactgga ctacacaata ggctggaaaa 420 gtgatccgca gagaggctca ttgctctaag ttcactccct gtaccaactg tcttgcacaa 480 agctgccacc cgggtgtctt cttccaacat ttcccctagt tggacttcaa agtttccttc 540 ttgcagcctg tgcggggacc aagaggccgg tctagagtag ccgcccagca tccagatccg 600 acatcctttt ccctttcctc aggaagactt ggatgcgcgc cagcccagcc cgggtctcca 660 ggttcagctg cggaagcttc ccacatggtg cccgtcgctt gggatgcggc tatccttgtg 720 ccttctctgc aggtgtcccg gcaggtagag gaggagaccg gtggctggtg ttcctgcagg 780 gcggggctgg ggctcctcga tgtccttgcg cttgccctgc aagttctgcg ccccaggccc 840 cggcagggac ggaaacaggc cgggaagcag tgacacctgg ggcagtcagt catccaggag 900 ccgccgccac ccgccccacc cccagtctcc gcgggaggtg tttgtcttcg cctatgctcc 960 cggctctttc tctttcactt ttcttttcgc caggggttgg gactccgggt ggcaggcgcc 1020 cgggggaatc ccagctgact cgctcactgc cttcgaagtc cggcgccccc cgggagggaa 1080 ctgggtggcc gcaccctccc 1100 // ID HSA_3601_IL15RA standard; DNA; HUM; 1100 BP. XX AC 3601; XX DT 05-Sep-2005 (Created) XX DE IL15RA: interleukin 15 receptor, alpha XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.10 6060049..6061148 (REVERSE) CC Score Points: 1 (50.0%) CC Chromosomal Location: 10p15-p14 XX CC Database Reference HGNC: 5978; IL15RA CC Database Reference ENTREZGENE: 3601 CC Database Reference UNIGENE: Hs.524117 CC Database Reference ENSEMBL: ENSG00000134470 CC Database Reference REFSEQ: NM_002189 CC Database Reference REFSEQ: NP_002180 CC Database Reference REFSEQ: NP_751950 CC Database Reference REFSEQ: NM_172200 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41677_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207375_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207375_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:495_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207375_s_at CC Database Reference TRANSFAC GENE: G014208; IL15RA XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="10" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 6060049..6061148" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000319465" XX SQ Sequence 1100 BP; 270 A; 250 C; 279 G; 301 T; 0 other; atgtccatag aataaaaaat gctctattgt atacatgcta tgcttagcct gcattcaata 60 aaccctcaat atatttgaga atattaagga atattgttaa tttttaaatt tgatcttatc 120 atcttgagat ttattattaa gtattgagag aaattgaata atgtgggatt tccccagttg 180 gagtaagggt ggctattcct gcttagaaaa aaagaatgga ccttgtgtgg tcactgccgg 240 atggtaggtt cattattctt tctacttttt ttttttaaat ttaagagaca ggaactggct 300 gtgttgccca ggctggagtg cagtggtgcg atctcagctc actgcaacct cagcctcctg 360 ggttcaagtg attctcctgc ctcagcctcc tgaatagctg ggattacagg cgcccgccac 420 catgcccagc taattttggt atttttagta gagatggggt ttcaccatgt tggccaggct 480 agtctcgaat tcctgacttc aggcgatcca cctgccttgg cctccgaaag tgcttggatt 540 tcaggagtgg ccaccgcgct cggccctaaa ttcttttatt taacttttaa gttcagggtt 600 ataagtgcag gtttgttata aaggtaaacc tgtgtcttgg gggattattg tacagattat 660 ttcgttttca aagagaattt gcaagtatgt cacaaaagcc tcataaacac gttgtgagat 720 tttaagaggc aatgaccgag gcttggagat gtctcgtcct gtccaatgtc accgctagac 780 ctgagaatct gcacttggga gcttacagac ccggttctca ggcttcactt gagaccccaa 840 gaaagaaaaa aacccaccag ccaaagagga ggatggcagc ctggaagaac ctaaggaagc 900 gaggctcaga ggtgaagcac tgtggctcct ctcccccttc tcccccctcc gccccctctc 960 cttctaagat gaggcatttt ctaggggagc aaagctgcag caggaattcg gcgaagtggc 1020 ggagctgggg ccccagcggg cgccgggggc cgcgggagcc agcaggtggc gggggctgcg 1080 ctccgcccgg gccagagcgc 1100 // ID HSA_3604_TNFRSF9 standard; DNA; HUM; 1100 BP. XX AC 3604; XX DT 06-Sep-2005 (Created) XX DE TNFRSF9: tumor necrosis factor receptor superfamily, member 9 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 7937392..7938491 (REVERSE) CC Score Points: 2 (66.7%) CC Chromosomal Location: 1p36 XX CC Database Reference HGNC: 11924; TNFRSF9 CC Database Reference ENTREZGENE: 3604 CC Database Reference UNIGENE: Hs.193418 CC Database Reference ENSEMBL: ENSG00000049249 CC Database Reference REFSEQ: NP_001552 CC Database Reference REFSEQ: NM_001561 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207536_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211786_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207536_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211786_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211786_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:31540_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207536_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 7937392..7938491" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:adKA01685" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 316 A; 214 C; 236 G; 334 T; 0 other; aaagtgttgc tgtcttgtcg gggtcatctc tgatttagtt tgagatggtt ttatggaata 60 gaaaaagctt ttgttgcatt tgaaagatta cagggctaca atggataaag caatatgata 120 catgttataa agcaaatgaa aattatacca aaagagtatt acacctttgg ctagcttaga 180 tagtatgtat atctggttaa ctatataatt tgacttagct tactacgatg attttatacc 240 acacaaaaat gcatgcagta acatgaattc tttttttttt tttttttgag acagtctagt 300 tttgttgctc aggctggagt gcacaggtgc aaacatggct gactgcaacc tcgacctccc 360 aggctcaagc aatcctccca tcccagcctc ccaagtagtt agaaccacag gcacatgcca 420 ccacacccag ctaatttttg tattttttgt agagacaggg tctgggcatc ttgtccaggt 480 catcttgaac tcttgggctc aagcgatcct cctgcctcag cctccctaag tgctgagatt 540 acaggtgtga gccactgttc ccagccatga attttttaaa cgcctgagta aagttgagca 600 tagccttcag tagcagaatt ctgaagtggt tgactttgtt taactgtggg ctggcaaaac 660 taatgttgag actcttttag ctcagtaaag actcttatgt tactggcata aaagcctgaa 720 atagtgagct aattactgtg ctgggaaact aaatatgtca ctttcagagg aagtaatgtc 780 tctgcctaca gaatgtccaa aacgtagact agtgagtagc atttagttaa atgaaatatg 840 gcccagttaa atgtcacact gcaatgttaa acagagtacc acatgtaaac aaggagatta 900 cttggttaga tggtgacttt caaagtgtta ggaggggatc agcagtccga tttttatggt 960 gtgacactct cacattcagc caatttctgc caaagtgggg caaggaggga tcccacagat 1020 gtcacaggta agataactct cagatgaccg tcagtatttg ggaacacatt ttgcaggcag 1080 ctcatgcgtt tttctccttt 1100 // ID HSA_3624_1_INHBA standard; DNA; HUM; 1100 BP. XX AC 3624_1; XX DT 06-Sep-2005 (Created) XX DE INHBA: inhibin, beta A (activin A, activin AB alpha polypeptide) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.7 41513222..41514321 (REVERSE) CC Score Points: 4 (19.0%) CC Chromosomal Location: 7p15-p13 XX CC Database Reference HGNC: 6066; INHBA CC Database Reference ENTREZGENE: 3624 CC Database Reference UNIGENE: Hs.28792 CC Database Reference ENSEMBL: ENSG00000122641 CC Database Reference REFSEQ: NP_002183 CC Database Reference REFSEQ: NM_002192 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210511_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210511_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40357_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204926_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204926_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210511_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204926_at CC Database Reference TRANSFAC GENE: G003125; INHBA XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="7" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 41513222..41514321" FT /note="Genomic Strand: REVERSE" FT prim_transcript 711..>711 FT /db_xref="dbTSS:STM02935" FT prim_transcript 1023..>1023 FT /db_xref="ENSEMBL:ENST00000242208" FT prim_transcript 1035..>1035 FT /db_xref="dbTSS:DMC07551" XX SQ Sequence 1100 BP; 271 A; 354 C; 188 G; 287 T; 0 other; ttatatgacc ccaaacaaaa gttccattgc gctctcctca gattgcctgc cagtgttgat 60 gacctgaaca tttaaatatg aatgaattgg gggaaaggac catctcccct ggatcccatc 120 aggccagaac aatcctctgt tacccctgag tccctcttcc ctgacctcca ctacctgtcc 180 actggacctc cctgcaccct ctgccccacc acgtggccag gtgggcgttc taccacctag 240 ggctgtggct tggctgggtg gaggggcggt gggaacactt tttcaatcaa ttcatcccta 300 ttgattgaga cactgtgttt gtttggggtt tcttttctcc cctccaaaaa aggaagaagg 360 tgaaaccagg agactgggca gagaaagaaa aaaaaatagt gaacaaaatt aggataattt 420 attttagaag agaaagtaga acccccgaaa atggtgatat ttgaagagag gtgtctgtga 480 ggaagctaag agcagaagga gagcagcctg tcagaaaacg ggctgtccct ccctccctaa 540 tcacagccct actcacagca aactccctcc ctctccattc actcacttac ttagggccaa 600 tcctttctct ctctctctct ctctctctct ctctctctct cttcctttcc ctctctccct 660 ctccccctcc cttccctccc tctctccctc tctctccccc ttctttccct ctctcttctc 720 tccccctctc tcctctctct ctgtctctgt ctccctccca tcctctctct ctgtctctgt 780 ctgtctcccc gccaccctgt ctctccctcc ctccctgtct ccctccctcc ctccctcctt 840 ccttctctct tactcggaga cagtcagaac tctcctccct gacagccaca aacctacagc 900 actgactgca ttcagagagg aacctgcaaa caaaacttca cagaaaactt tttgttcttg 960 ttccagagaa tttgctgaag aggagaagga aaaaaaaaac accaaaaaaa aaaataaaaa 1020 aatccacaca cacaaaaaaa cctgcgcgtg aggggggagg aaaagcaggg ccttttaaaa 1080 aggcaatcac aacaactttt 1100 // ID HSA_3627_CXCL10 standard; DNA; HUM; 1100 BP. XX AC 3627; XX DT 06-Sep-2005 (Created) XX DE CXCL10: chemokine (C-X-C motif) ligand 10 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 77301730..77302829 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 4q21 XX CC Database Reference HGNC: 10637; CXCL10 CC Database Reference ENTREZGENE: 3627 CC Database Reference UNIGENE: Hs.413924 CC Database Reference ENSEMBL: ENSG00000169245 CC Database Reference REFSEQ: NP_001556 CC Database Reference REFSEQ: NM_001565 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204533_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204533_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204533_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:431_at CC Database Reference TRANSFAC GENE: G005973; CXCL10 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 77301730..77302829" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000306602" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [245920]; Alignment" XX SQ Sequence 1100 BP; 334 A; 228 C; 182 G; 356 T; 0 other; attaagtttt gccacgattc atcatccagt taaaattgtg ccaatttcag ttatcactgt 60 tactagctca atggccaaca cttttttttt ctttttcttt gcatttaaca gtgtcttgga 120 gctgaacccc atcgtaaatc aacctgtttc ccttctgtct caagctactt tcccaaggtc 180 tgtctctatg cgtgcccccc cgcttttaaa ttcatttcct caaaaagcac cctttgtttt 240 ttacaataac cctaggatag ctatgaatcc ttttctcaca ccattctaga taccatctta 300 tgatgttttc attcagggac tgctataaga cgtgaaactt gttttaacac accacaaatc 360 agatacccaa atgagcaatg ttttccctca aaatagttat gttggaggct atttacttaa 420 tctaatggtg ttatgaatga tcaaagcatt tattgaatta tttaaaactt gccagttcca 480 gatctttgac cctgtcaaag caggccagtc ctattacttt atagtatttg atcaaggagg 540 actgtccagg taaatcactg ttctaataat caggcacaac ttgctgttac caaaaaatta 600 ggtttaccta taaaggatga aaaatttcta ttactgggga tattttgaaa aataacctct 660 gaaagtaact gtaaaagttt aagtgttgag aaaaagcatt atagttagaa tggattgcaa 720 cctttgtttt tttctatatg caatgaagtt ctttttttca agaaacagtt catgttttgg 780 aaagtgaaac ctaattcact attaccaaaa aaagaggagc agagggaaat tccgtaactt 840 ggaggctaca ataaataata ccttcgagtc tgcaacatgg gacttcccca ggaacagcca 900 gcaggttttg ctaagtcaac tgtaatgccc ttatccaatc agaattaggg agggaaaatg 960 gctttgcaga taaatatggc acactagccc cacgttttct gagacattcc tcaattgctt 1020 agacatattc tgagcctaca gcagaggaac ctccagtctc agcaccatga atcaaactgc 1080 cattctgatt tgctgcctta 1100 // ID HSA_3659_IRF1 standard; DNA; HUM; 1100 BP. XX AC 3659; XX DT 06-Sep-2005 (Created) XX DE IRF1: interferon regulatory factor 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 131854252..131855351 (REVERSE) CC Score Points: 51 (98.1%) CC Chromosomal Location: 5q31.1 XX CC Database Reference HGNC: 6116; IRF1 CC Database Reference ENTREZGENE: 3659 CC Database Reference UNIGENE: Hs.436061 CC Database Reference ENSEMBL: ENSG00000125347 CC Database Reference REFSEQ: NP_002189 CC Database Reference REFSEQ: NM_002198 CC Database Reference AFFYMETRIX: AFFY_HG_U133B:238725_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:59777_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202531_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:238725_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:669_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202531_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202531_at CC Database Reference TRANSFAC GENE: G000324; IRF-1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 131854252..131855351" FT /note="Genomic Strand: REVERSE" FT misc_signal 857..883 FT /note="TRANSFAC Site R12315" FT misc_signal 859..879 FT /note="TRANSFAC Site R04223" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP74545" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [16362]; Alignment" FT /note="PRIMARY ANCHOR: RNO [24508]; Alignment" FT prim_transcript 1019..>1019 FT /db_xref="ENSEMBL:ENST00000245414" XX SQ Sequence 1100 BP; 196 A; 355 C; 366 G; 183 T; 0 other; tgctaggagg gatcagagct agcccacccc taccctcact cagccgtctg ggcttctctg 60 aaccccttct cctcctctgt tccctaaagc cagccagggg gagtcccagg gaggcagacc 120 gaaaaggggt ggggtgtcat cctggtcact attagaccct gcaacggcga ccttgaaaac 180 tactcagcgt ctgttgcccg agtggagcat agtgctttac aatctcttcc catcacagca 240 aaccatcaag gtagggctac tattatttta tggttgaaaa acagaggtcc tgcgtccctt 300 gggggctgtg ccagcagcgg ccaagttggg atttcccctg gtccagcagc cccagacagc 360 acacggggca gggtaggctt tctgccttct tcacttcccc agggcaggtg agtgacctgg 420 agggaggggg tcacccctaa aaacaggggt agtgctagga ctgaaaccct cccttcttga 480 tatcccactg gcaagcttga ggagccaggc tgccagtcgg gagattcggc ccagtgttcc 540 cactggagag ggcggcaagt gcccgggcga tcccctcacc tgcgttcggg agatataccc 600 ccgcccccgc cccgccagga gggtgaaaag atggccccag gagccagccg gctgggacaa 660 ggcggagtga gaggacaggc tggggccagg ggcgctgggc tgtcccgggc agccctcctc 720 cgggcaagcc ggagcagggg tggattggga gcgctcgggg cgggcccgcg gtggccccgg 780 ggcggtggcg cccggccgga gagggtgggg cggagcagcc gccctgtact tccccttcgc 840 cgctagctct acaacagcct gatttccccg aaatgacggc acgcagccgg ccaatgggcg 900 cccgcgcggc tgtccggggg cggggccggc cagggctggg gaatcccgct aagtgtttgg 960 attgctcggt ggcgccgctg ccctggcaga gctcgccact ccttagtcga ggcaagacgt 1020 gcgcccgagc cccgccgaac cgaggccacc cggagccgtg cccagtccac gccggccgtg 1080 cccggcggcc ttaagaaccc 1100 // ID HSA_3660_IRF2 standard; DNA; HUM; 1100 BP. XX AC 3660; XX DT 06-Sep-2005 (Created) XX DE IRF2: interferon regulatory factor 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 185770696..185771795 (REVERSE) CC Score Points: 60 (98.4%) CC Chromosomal Location: 4q34.1-q35.1 XX CC Database Reference HGNC: 6117; IRF2 CC Database Reference ENTREZGENE: 3660 CC Database Reference UNIGENE: Hs.374097 CC Database Reference ENSEMBL: ENSG00000168310 CC Database Reference REFSEQ: NM_002199 CC Database Reference REFSEQ: NP_002190 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1220_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:42723_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203275_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203275_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203275_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1219_at CC Database Reference TRANSFAC GENE: G001056; IRF-2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 185770696..185771795" FT /note="Genomic Strand: REVERSE" FT prim_transcript 921..>921 FT /db_xref="dbTSS:AMR04161" FT prim_transcript 927..>927 FT /db_xref="dbTSS:KAR04937" FT prim_transcript 942..>942 FT /db_xref="dbTSS:Zrv61130.seq" FT prim_transcript 944..>944 FT /db_xref="ENSEMBL:ENST00000303389" FT /db_xref="dbTSS:PCD00485" FT prim_transcript 945..>945 FT /db_xref="dbTSS:KGR09425" FT /note="Number of reported TSSs: 2" FT prim_transcript 947..>947 FT /db_xref="dbTSS:PNC05572" FT prim_transcript 956..>956 FT /db_xref="dbTSS:ADB00438" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:HCR04385" FT prim_transcript 1012..>1012 FT /db_xref="EPD:EP48006" XX SQ Sequence 1100 BP; 209 A; 335 C; 328 G; 228 T; 0 other; tggttgaaaa ccgaggccaa gggtgaccag ccagtgagtt aaggaggccc cagccgaact 60 ttgctggaag tgctccagca taaagcctct ctccagaacc agccgccact gagacgtctt 120 gaagtcaaag taactcacac ccttgtccac ctcgccctgc ggtgaagaaa cttcggtcgc 180 acaggctcca gaactcatct tggcgtgggc tgtgacttac tgggggatgg gcctcctttt 240 cgttctagct cctaaatgga gcggagcgcc aggtggtgtc agagggggcg gcggcccctc 300 caatggtggc accctcagcc acggataagg ttccaattag gtaaggacgc aagtaatgct 360 gtcgtttcgg ctgactgctc ctttcattcc ttggaggtgg tcggtgtcac aaaacgaatt 420 ttcatttact ctcaacagtc acaccagccc tgctaactgg atggtcgcag ccccgtgcct 480 tcgccggacg ccctcctgga accttcaggc caccctgagg atggagactc gggtgcccgc 540 tctcctcccc taccgccgcg ggcctgcgcc ccccgccccg gaccccgact cggacgttct 600 agccgcacgt gcgggcgccc ctgggtgcga gccgcggact cacgagccgc tgcttgttgc 660 tcccgccgcc gcgacctggg gaagcgaaaa tgaaattgac ttttccgaga aatgatgaaa 720 gcggcgctgc ccgccaatga gctgctgcgg cgaacttccg cacctcccgg ccgggccgct 780 cgcgccctcc ctccgcctcc acctcccggt tgcacaagct tgaaacaaac actggggagg 840 aagggcggag ggaggagggc ggagagggga ggcgagggag ggagcgcggc cggaggaggg 900 cggggggtgg ggggatttcc agccgcggct cttcgcagtt tcctctcctt gttttgcttt 960 cgatctggac tgttctcagg caagccgggg agtaactttt agttttgctc ctgcgattat 1020 tcaactgacg ggctttcatt tccatttcac ataccctagc aacacttata ccttgcggaa 1080 ttgtattggt agcgtgaaaa 1100 // ID HSA_3669_ISG20 standard; DNA; HUM; 1100 BP. XX AC 3669; XX DT 06-Sep-2005 (Created) XX DE ISG20: interferon stimulated exonuclease gene 20kDa XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.15 86982131..86983230 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 15q26 XX CC Database Reference HGNC: 6130; ISG20 CC Database Reference ENTREZGENE: 3669 CC Database Reference UNIGENE: Hs.459265 CC Database Reference ENSEMBL: ENSG00000172183 CC Database Reference REFSEQ: NP_002192 CC Database Reference REFSEQ: NM_002201 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:33304_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33304_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:33304_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204698_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204698_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204698_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:90103_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:33304_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="15" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 86982131..86983230" FT /note="Genomic Strand: FORWARD" FT misc_feature 750 FT /note="SECONDARY ANCHOR: MMU [57444]; Alignment" FT prim_transcript 913..>913 FT /db_xref="ENSEMBL:ENST00000306072" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [57444]; Alignment" FT prim_transcript 1089..>1089 FT /db_xref="dbTSS:STM03912" XX SQ Sequence 1100 BP; 267 A; 289 C; 293 G; 251 T; 0 other; ctgaattaaa gcaaaagttg cttattcagg atgggaatca aaaactctca cacctcaaat 60 ttgcatccag tgaacagtaa gcaggagcag ggctttctca tgaagacgta tttcagtctt 120 tggttttatt tttgaggttt gttaaagttg ggcatccaaa tcccacttgg tgaaaatact 180 acagacctgg ggaagttact tttcaaacca cagatcttca tgacactggg aggcagtcag 240 attggaggga tcagtgtgga ttctgcacag atctggggta ggaggcaagc gtgggtaacg 300 ctcagcttat tgttggatct caccacagtg aaagacaagc acttccctca ttgaaagttg 360 attttctttt tgccccagtt gtaactcatt tgacattcac taaataccaa gccctcccta 420 tctggcaggc actgttctaa gagctcaaag tcctagcctg ggagagtgtg gacccaagga 480 agtgtggccg ggctggtggg gcctccccga aggcctgctt ctccttcacc ctcacagagt 540 cagccccact ggaggcagag ctcattgagg catctggaac ccacggaggc ctgtaagggc 600 tccctcgctg ctccttgcct tccctgggtt ggaagtgggg gctagccact cccaccacaa 660 gtttctcctg cccattccaa taaaagcctg tatgtcccaa gagccagctt ccctacccca 720 taagagacca ctgagtatca gactggtagc aggctccaga agttagttgt gggacattcc 780 ctgagctcca gtcctgggga tgtttattct ctgggcggag ggtgagaaag gaaacaaaga 840 tgttgcaatc cactccacga acgtcaaatg cgtcatctga ggagggggag ggccggggca 900 aaggaggggc accctgacat ggagcctgcc agctccgtca gccctgactc ggcccggagc 960 tgagctcccc acctgccggt agcccaggag atggagcagc ccagcccacg tgcccggcct 1020 tccgcccctg acttcacttg ataacaaact agaaactgaa acagggtcgg gatgccgatg 1080 ccggcttgga gttagagatg 1100 // ID HSA_3726_JUNB standard; DNA; HUM; 1100 BP. XX AC 3726; XX DT 06-Sep-2005 (Created) XX DE JUNB: jun B proto-oncogene XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.19 12762299..12763398 (FORWARD) CC Score Points: 13 (92.9%) CC Chromosomal Location: 19p13.2 XX CC Database Reference HGNC: 6205; JUNB CC Database Reference ENTREZGENE: 3726 CC Database Reference UNIGENE: Hs.25292 CC Database Reference ENSEMBL: ENSG00000171223 CC Database Reference REFSEQ: NP_002220 CC Database Reference REFSEQ: NM_002229 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201473_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201473_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:2049_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201473_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32786_at CC Database Reference TRANSFAC GENE: G006329; JUNB XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="19" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 12762299..12763398" FT /note="Genomic Strand: FORWARD" FT misc_feature <1..238 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT prim_transcript 993..>993 FT /db_xref="dbTSS:adSH01557" FT prim_transcript 996..>996 FT /db_xref="dbTSS:adKA03272" FT prim_transcript 998..>998 FT /db_xref="dbTSS:adKA01458" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:ADG08022" FT /note="Number of reported TSSs: 4" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [24517]; Alignment" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:KDN07277" FT /note="Number of reported TSSs: 3" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:PRS03834" FT prim_transcript 1006..>1006 FT /db_xref="dbTSS:COL06279" FT prim_transcript 1012..>1012 FT /db_xref="ENSEMBL:ENST00000302754" FT misc_feature 1020 FT /note="SECONDARY ANCHOR: RNO [24517]; Alignment" XX SQ Sequence 1100 BP; 193 A; 384 C; 274 G; 249 T; 0 other; ggggacagag aatacagatg actaagaggt taccatcgag ggggagcagc agtcgtggaa 60 gatccagcag tcctggtgcg cgggaccctc aaggccccct cctcacatgt caactgagta 120 ccctcttatt gtcttctctg ctccgaagat gtgtccggcc ccttctaact ctctccttca 180 tccgggctag cagatgaccc cagtggtccc caatttctgg cagacatgtc tccatcttct 240 acctggcata ttttacctgc ctcagtgtac cccaggccgc ttactagctt tctgcatatc 300 tagacttccc ctaatgcctc cttcccgctt acgggagagc ctcagactct ggactcagct 360 cccatgagct cctggacccc tactcatttc ttgcaattta atgggtcatg cagctccacc 420 cactcacccc ttttgatctc tcccctcctc cgtcctgtga aaattccagt cccgcatcct 480 tctgagcccg ggacccccag tcaattcctg ggtcaggtgt ctccttaacc ctcccgattt 540 acagtgctta accctcattt ctgctttttg gggtctccca atggattgtc agtcctccta 600 cccctctcgt attctgggta cctcaggggt ttcttcgcac atactgggac cctcacccca 660 cttgctgcgt accaggtcct ggtatttgtc ccagtggact ccagggaaat catcctcctc 720 cctgaaaccc ctcactcatg tgcctgggcc ccccagcacc tccttccatg cgtaccccga 780 ggtcctttga gcccctcccc ctgcagcccc gccgagccac ccggcccgtg gccgctgttt 840 acaaggacac gcgcttcctg acagtgacgc gagccgcctc ctccccttcc ccacgctcga 900 ggaggggggc gcgggggccc ggctccggcg acggccaatc ggagcgcact tccgtggctg 960 actagcgcgg tataaaggcg tgtggctcag gctgagcggc tgggaccttg agagcggcca 1020 ggccagcctc ggagccagca gggagctggg agctggggga aacgacgcca ggaaagctat 1080 cgcgccagag agggcgacgg 1100 // ID HSA_3918_LAMC2 standard; DNA; HUM; 1100 BP. XX AC 3918; XX DT 06-Sep-2005 (Created) XX DE LAMC2: laminin, gamma 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 179886056..179887155 (FORWARD) CC Score Points: 1 (25.0%) CC Chromosomal Location: 1q25-q31 XX CC Database Reference HGNC: 6493; LAMC2 CC Database Reference ENTREZGENE: 3918 CC Database Reference UNIGENE: Hs.530509 CC Database Reference ENSEMBL: ENSG00000058085 CC Database Reference REFSEQ: NP_005553 CC Database Reference REFSEQ: NM_005562 CC Database Reference REFSEQ: NM_018891 CC Database Reference REFSEQ: NP_061486 CC Database Reference AFFYMETRIX: AFFY_HG_U95E:86529_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35280_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202267_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202267_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202267_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 179886056..179887155" FT /note="Genomic Strand: FORWARD" FT misc_feature 439..>1100 FT /note="ChIP-on-Chip Fragment: HNF6_panc" FT /note="PubMed:14988562" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000264144" FT misc_feature 1090 FT /note="SECONDARY ANCHOR: MMU [16782]; Alignment" XX SQ Sequence 1100 BP; 272 A; 272 C; 318 G; 238 T; 0 other; tcctctttct tattcatttc aagccaatat ttattaagca ccaactgcaa gctagatact 60 attatagtta ggaatataaa gtgggccagg gatggtgttt atgcctataa tcccagcact 120 ttgggaggcc aaggcaggag gattacttga ggccaggaat tcaaggtcag cctgcccaac 180 acagcaagac ctcgtctcta caaaaaatta aaaaattagc tgggtgtggt ggcatttgcc 240 tgtagcccta gctactcaag aggctgaggt gggaggattg cttgagccca ggggttggag 300 gctgcagtgc gctatgatgg tgccattgaa aacaaaaaca aaaaccaacc aacaaacaaa 360 aaaacaaaca aaaagaaaac gatactcagt ctttataggg aggttggcca gtcaataggt 420 tactttatga gttgctaacc ctggtgagca ggaagttatg tggaccagga gagaaaccct 480 tggttcagcc tggagaaagg agaggttgac cctaaactgg agggtggaga ggaccctgtt 540 gtgactctcc gactgacttg tcttccttga tgtcctttaa gccggagctg attcgggctg 600 ctgccttatt tctgagttag cgctcttaag attgggcctc ccagtttgag gaaggggcgg 660 gctgctgtct acctctgtga atctgccctg gaccaccccg ggagagaagg agggctccgg 720 ggaatctcgc acattccagg caaaggctcc cgggccgcag cctctgtgcc acacccttgg 780 cccgggccag gtgtgcgccc tcctcgctgc gagggggagc gggcggctgc ggggagcgat 840 tttccagccc ggtttgtgct ctgtgtgttt gtctgcctct ggagggctgg gtcctcctta 900 ttcacaggtg agtcacaccc tgaaacacag gctctcttcc tgtcaggact gagtcaggta 960 gaagagtcga taaaaccacc tgatcaagga aaaggaaggc acagcggagc gcagagtgag 1020 aaccaccaac cgaggcgccg ggcagcgacc cctgcagcgg agacagagac tgagcggccc 1080 ggccccgcca tgcctgcgct 1100 // ID HSA_4050_LTB standard; DNA; HUM; 1100 BP. XX AC 4050; XX DT 06-Sep-2005 (Created) XX DE LTB: lymphotoxin beta (TNF superfamily, member 3) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 31661624..31662723 (REVERSE) CC Score Points: 1 (33.3%) CC Chromosomal Location: 6p21.3 XX CC Database Reference HGNC: 6711; LTB CC Database Reference ENTREZGENE: 4050 CC Database Reference UNIGENE: Hs.376208 CC Database Reference ENSEMBL: ENSG00000096158 CC Database Reference REFSEQ: NP_033666 CC Database Reference REFSEQ: NP_002332 CC Database Reference REFSEQ: NM_009588 CC Database Reference REFSEQ: NM_002341 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207339_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40729_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207339_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207339_s_at CC Database Reference TRANSFAC GENE: G003179; LTB XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 31661624..31662723" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000359189" XX SQ Sequence 1100 BP; 209 A; 304 C; 315 G; 272 T; 0 other; ccagcccttt cctctgccct gggctgacca cgtggtttgg aggggacttt tcagccctgg 60 atggttctag gtgctggtaa ggggatgatg gaggggaagg agcctgggcc tgggtgggtg 120 tgggcactgg ggggaagaag ggagggtgat atcagcacac ccagcaggtg ggctgctccc 180 tgagccgcag agcagcgcgg gagtgtgggg gcccccttgg ctggtgtgga gagctgcttc 240 ccacaggcag atgctgctag ggctgaagtg gggcatggag gagtatctgg ggccccataa 300 cttcccctca ggcacttcct cccctccaac cactggttcc tgtttgaggg tgaagagggg 360 gccgttctct tcaccccaga gccagatata ctgactaggg tctggaaact gggacccttc 420 tgggtttaag aggaattctg gggggtgggg agcagaagtg caggtggagg ccataagggc 480 cgtgggcaca gaaatgaatt gtctttaatt tctttgggga gcagagactc agaggattcc 540 tcgacggccc agggaaactc aaacccatac tctccctccc ctcatcttag cttcacccca 600 ctctggggtg tgaccatcct tccaccaagg tccctgccca ttcccagctt acccagagct 660 tgtggcctgc aggatggaca gactccaaac tggccagtgc tgtctggctg aagagaagtg 720 ttgccacctc agacattcct gcccctcctc tggctttaac ttctccccca gcctgggttc 780 ctccccagca ttgttaggag aggaagttcg gctccagggt tagggttaca acatctttct 840 tttcaaactt ctgggcctgt agctagggcc ataatctgcc tcagctccag tcatttcact 900 gatcctgcca ctagtcagca aacacccacc accttcaggt gtcttccttg attaactctt 960 ctctattacc tcttacactg catctgttga gacctcttga tcttggcata tgtctgtgga 1020 cacatgtacc ctgctccagt tcagactggg agctctggca tatttggtgt tctggtgacc 1080 cacttggtgt tctgcagctc 1100 // ID HSA_4088_SMAD3 standard; DNA; HUM; 1100 BP. XX AC 4088; XX DT 06-Sep-2005 (Created) XX DE SMAD3: SMAD, mothers against DPP homolog 3 (Drosophila) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.15 65144331..65145430 (FORWARD) CC Score Points: 1 (20.0%) CC Chromosomal Location: 15q22.33 XX CC Database Reference HGNC: 6769; SMAD3 CC Database Reference ENTREZGENE: 4088 CC Database Reference UNIGENE: Hs.36915 CC Database Reference UNIGENE: Hs.549051 CC Database Reference UNIGENE: Hs.555881 CC Database Reference ENSEMBL: ENSG00000166949 CC Database Reference REFSEQ: NP_005893 CC Database Reference REFSEQ: NM_005902 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205396_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38944_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1950_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205398_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:51059_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205396_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205397_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1454_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205397_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205398_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:58763_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205398_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205397_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1433_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205396_at CC Database Reference TRANSFAC GENE: G002399; SMAD3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="15" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 65144331..65145430" FT /note="Genomic Strand: FORWARD" FT misc_feature 858 FT /note="SECONDARY ANCHOR: MMU [17127]; Alignment" FT misc_feature 987 FT /note="SECONDARY ANCHOR: RNO [25631]; Alignment" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000327367" XX SQ Sequence 1100 BP; 147 A; 410 C; 404 G; 139 T; 0 other; aggttgtcac tggtgtcccc agctctccac ttctgaggac ccacttctca ccccctcctc 60 ctccgcacac gttcccgagg ctctcggccg gtgtgatctc accgactaga gaataaaaac 120 agcccagggg cgccggcgcc ggccaagggc cttgacgggg atcagcaagc gcgaggccaa 180 gtgcgggccc caacttcctg ggcccgggcc ttccgcgcgc cccctctcgg gctcgggtcc 240 tctccagggt gcactcgcgt ccggacgacg cttacttgct gcgagtccaa ccctctccgg 300 cccgcaactc caaccgagcc gcccgagtgt ggactccgag agcggacgcc acgggccgcg 360 ctcagccctc ccgcccgagg cccctctcgc cgtgtttccc aggacttcct ccccgcgccc 420 gcccgacttc aggtcggggc cgcgcagggt cccgcgcgct ccagccagga ctgccgccgc 480 ccgggtcgcc cacgtgggcg tgctgggcgc ggggtggtgg ccggccgggc gccctccccg 540 gagcaggggg cgggcagggc gcccgcggga ggaggtggcg gggcgcgggg gaggaggcgg 600 ggagccccgg cggcgagggg gcggtgacag cacttggaaa ggaggctgca cgcggatttg 660 catgaaacac agactgggag cgggcgggag cgggagcgcg gcgcacgccc cgggccggcc 720 cagccagcga gcgagcgagc ggcgagccgg gaggaggagg gtggcggggc ggtgaggccg 780 cagaggcgga gggatctgcg catcaaagct agcgaggcga gcgaagtttg gccgggggtt 840 ggactttcct tcccggaggc ggcacccaaa cagctacccc gtgcggaaac ccaaacttct 900 gctgccactt ggagtctcgc ggccgccgcc tccgccccgc gttcggggcc ttcccgaccc 960 tgcactgctg ccgtccgccc gcccggccgc tcttctcttc gccgtgggag ccgctccggg 1020 cgcagggccg cgcgccgagc cccgcaggct gcagcgccgc ggcccggccc ggcgccccgg 1080 caacttcgcc gagagttgag 1100 // ID HSA_4319_MMP10 standard; DNA; HUM; 1100 BP. XX AC 4319; XX DT 06-Sep-2005 (Created) XX DE MMP10: matrix metallopeptidase 10 (stromelysin 2) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.11 102156469..102157568 (REVERSE) CC Score Points: 21 (95.5%) CC Chromosomal Location: 11q22.3 XX CC Database Reference HGNC: 7156; MMP10 CC Database Reference ENTREZGENE: 4319 CC Database Reference UNIGENE: Hs.2258 CC Database Reference ENSEMBL: ENSG00000166670 CC Database Reference REFSEQ: NP_002416 CC Database Reference REFSEQ: NM_002425 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205680_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1006_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205680_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205680_at CC Database Reference TRANSFAC GENE: G003076; MMP10 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="11" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 102156469..102157568" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:CAS05488" FT /note="Number of reported TSSs: 18" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:T3R01943" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [17384]; Alignment" FT /note="PRIMARY ANCHOR: RNO [117061]; Alignment" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:T3R02933" FT prim_transcript 1013..>1013 FT /db_xref="ENSEMBL:ENST00000279441" XX SQ Sequence 1100 BP; 365 A; 186 C; 199 G; 350 T; 0 other; ttaatttatc tttagtgaga gaaaaatata gttctttact ataagaattt cagggttctt 60 tatattaaca ggttaatttg acaaaacagt tattgcagac ttactgtgtt actgcgtaaa 120 aagcacttta tttggctgag aaaacaagaa agaaaatact atttgtgggc aggggtggat 180 cgttagacat gtgaaagaaa gggaggattt gaaatcattt cccattacag atctcaatcc 240 atctcctcct ttgtacctta agaggagaaa gaaaggggga aaagaatttt taaaagcaaa 300 gaagaggaag agggtaggag gaccatttca gtctaacatg caatttaatt ttttccattt 360 aacaagtttt atggagcagt tactttgaac ataattatac actgggaaat ggagaatgag 420 tgaacaccaa agcttctctc tttggattct tttctctaca tgctccatgt ccttctcaca 480 atacccctac tccacggcca gtaaatccat ctgaaaatca ataatagcta ttgtaaacaa 540 ggactcaaga agtgaaatat ttgttttaat atctttgtaa ataacaactc ccacatttag 600 accacgacta tatttggaat ttatttccgt tgacctactt aattcttacc tgcttatatt 660 taagtttaaa acataatctt cttaaaagaa aattgcactg attttaaaat gtcaaaacat 720 ttggcatttt accaagcttg tcagctctct ttaagtaaat acagagacgt gaattatcta 780 gccaattctt tttcgtcttt acaaacacag aaatcatttc ctggggatta atcattcttt 840 caagtttaga aagttgaagg aaaatactga tgtaggctgt atcaccatta cattaaatgt 900 ttgtgaacat tcagacttaa aaaacacatg catgaatcat actgttggtg atctcagcat 960 tgtctctgta taaaagaaag gccactaggg ggtagagcta gaagcccagt agacaaagaa 1020 ggtaagggca gtgagaatga tgcatcttgc attccttgtg ctgttgtgtc tgccagtctg 1080 ctctgcctat cctctgagtg 1100 // ID HSA_4487_MSX1 standard; DNA; HUM; 1100 BP. XX AC 4487; XX DT 05-Sep-2005 (Created) XX DE MSX1: msh homeo box homolog 1 (Drosophila) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 4978478..4979577 (FORWARD) CC Score Points: 1 (50.0%) CC Chromosomal Location: 4p16.3-p16.1 XX CC Database Reference HGNC: 7391; MSX1 CC Database Reference ENTREZGENE: 4487 CC Database Reference UNIGENE: Hs.424414 CC Database Reference ENSEMBL: ENSG00000163132 CC Database Reference REFSEQ: NM_002448 CC Database Reference REFSEQ: NP_002439 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40199_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205932_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:214_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205932_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:215_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:82705_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205932_s_at CC Database Reference TRANSFAC GENE: G003978; MSX1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 4978478..4979577" FT /note="Genomic Strand: FORWARD" FT misc_feature 987 FT /note="SECONDARY ANCHOR: MMU [17701]; Alignment" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000295284" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [81710]; Alignment" XX SQ Sequence 1100 BP; 279 A; 266 C; 346 G; 209 T; 0 other; agagataggg acatgtcatt gtttccgagg acgcgttgtt tgaggtcacc ttaaggccag 60 atcggtgttt cattgacgat tctgttggtt ttatttcagt aagttctata tcaaaaggat 120 ctggcagctc ctttccccgc ccgggcgcta taggtgttgt gacccttggg acagaagttc 180 agagcgaggg tggggggggg ggaatacaca tcgtgtatga aaaccgactg cagattctag 240 ataatcttac gtattctcac atccttggca ctacaggaag ctagcttctt cccgcaaggt 300 ttactccagc tctaagttag agacaaaggc ccacttttac ctcgaggtaa agtttacaag 360 atttcagaac aggaagaaaa tgaaggtttg gttttgtttc gtttcttgaa aagaagttaa 420 tagtatgtct ttctcctagg ataaatagcc atgcgtattt taaaaactat atataaaagg 480 aatgtgtaag aaataacctc aactcaaatt attgtggtag aagaagaggg ggggtcagac 540 agtggagggg ggcacaggga aacccagcca cagactaaag agaaaggtaa aagaagcagt 600 agaggagaga aacaaggacg gggaaaaaaa gaggagcgga aaagagggct gaggagggga 660 ggggagggga ggagaggagg gcagaagaga aggaacgaga acaagggaaa atcccccggg 720 aacacagaaa gatagagacc caggggactc ccgcagagag ggcctcttgg gcttcagcgc 780 agaggaaagt ttcccgggca ccccctctcc tcccctgccc tccgccgcct gggccctgcc 840 ctgcgtgccc ccaggcccag cgcgcctccg ggcgagtccc caggagcgcg gcccaatgga 900 tcgctccggg cccgccccct cgcgcgctga ttggccgccg ccccgctggc ctcgccttat 960 tagcaagttc tctggggagc cgcggtaggg cccggagccg gcgagtgctc ccgggaactc 1020 tgcctgcgcg gcggcagcga ccggaggcca ggcccagcac gccggagctg gcctgctggg 1080 gaggggcggg aggcgcgcgc 1100 // ID HSA_467_ATF3 standard; DNA; HUM; 1100 BP. XX AC 467; XX DT 07-Sep-2005 (Created) XX DE ATF3: activating transcription factor 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 209169507..209170606 (FORWARD) CC Score Points: 1 (33.3%) CC Chromosomal Location: 1q32.3 XX CC Database Reference HGNC: 785; ATF3 CC Database Reference ENTREZGENE: 467 CC Database Reference UNIGENE: Hs.460 CC Database Reference ENSEMBL: ENSG00000162772 CC Database Reference REFSEQ: NM_001030287 CC Database Reference REFSEQ: NP_001025458 CC Database Reference REFSEQ: NM_001674 CC Database Reference REFSEQ: NP_001665 CC Database Reference REFSEQ: NM_004024 CC Database Reference REFSEQ: NP_004015 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1554420_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202672_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202672_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202672_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1554980_a_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:287_at CC Database Reference TRANSFAC GENE: G002871; ATF3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 209169507..209170606" FT /note="Genomic Strand: FORWARD" FT misc_signal 902..909 FT /note="TRANSFAC Site R11553" FT misc_feature 905 FT /note="SECONDARY ANCHOR: MMU [11910]; Alignment" FT misc_signal 968..984 FT /note="TRANSFAC Site R11477" FT misc_feature 995 FT /note="SECONDARY ANCHOR: RNO [25389]; Alignment" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000341491" XX SQ Sequence 1100 BP; 178 A; 393 C; 310 G; 219 T; 0 other; ccctcctcct ggccgctggc ttccgccccc tcctaccctc ccaccgggtt gcctctgatt 60 cctcctggac tccgatcttt tcacgctctt gttggtttca ctgacatgtt cttgtcaatt 120 tcaaacgctt tgtgattgta aaaaaaaaaa aatcgaaccg atacggtcct accactcgcc 180 ctagtttcgg agcccggagc tgtcctgcgt gtgcgtccat gtggagtgtc cggggctgcg 240 ggctcgggcg cacggtgcca gccgagggct gccctccgct tttgtgttaa ccggcgggct 300 tctcgcggtc cccgccgcag aggtcacacc cggcgggtaa cggcgtggat acaccgaagg 360 gtgactttgg acaccttccc cacaccacag actaacgctt ctgcccctac tccgcccctg 420 ctagagaagt aggaggccag tgggggaggg ggtattttcc tgaagctcca gaaaatgacc 480 acgcatttta gagaaaggtc gtgcccgctt cccagcctca cctagtctgg gctggggccg 540 ggacccgcct ccccaccttc cccgcccccc ccgctcttca acctagcgga gggacagatg 600 ccagcgcggt ggagtcatgc cgctggcttg ggcaccattg gtcatgcctg gaacacgcag 660 cagcgagtac gcacatctgg cggctatccc gggcggctcc ggtcctgata tggagagaga 720 gggcgggctg gtgtgtgtct cagtgagcga ggctggggga acgcgcctgg gctggctcct 780 ccccgaactt gcatcaccag tgccccctct ctccacccgc cttcggcccc gccttggccc 840 ctcctccacc ccccttcctc cgctccgttc ggccggttct cccgggaagc tattaatagc 900 attacgtcag cctgggactg gcaacacgga gtaaacgacc gcgccgccag cctgagggct 960 ataaaagggg tgatgcaacg ctctccaagc cacagtcgca cgcagccagg cgcgcactgc 1020 acagctctct tctctcgccg ccgcccgagc gcacccttca gcccgcgcgc cggccgtgag 1080 tcctcggtgc tcgcccgccg 1100 // ID HSA_4791_NFKB2 standard; DNA; HUM; 1100 BP. XX AC 4791; XX DT 06-Sep-2005 (Created) XX DE NFKB2: nuclear factor of kappa light polypeptide gene enhancer in DE B-cells 2 (p49/p100) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.10 104143265..104144364 (FORWARD) CC Score Points: 2 (28.6%) CC Chromosomal Location: 10q24 XX CC Database Reference HGNC: 7795; NFKB2 CC Database Reference ENTREZGENE: 4791 CC Database Reference UNIGENE: Hs.73090 CC Database Reference ENSEMBL: ENSG00000077150 CC Database Reference REFSEQ: NM_002502 CC Database Reference REFSEQ: NP_002493 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40362_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:544_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207535_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207535_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:535_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209636_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209636_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207535_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:545_g_at CC Database Reference TRANSFAC GENE: G006466; NFKB2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="10" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 104143265..104144364" FT /note="Genomic Strand: FORWARD" FT prim_transcript 945..>945 FT /db_xref="dbTSS:HEP05934" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [18034]; Alignment" FT prim_transcript 1056..>1056 FT /db_xref="ENSEMBL:ENST00000336486" FT misc_feature 1063 FT /note="SECONDARY ANCHOR: MMU [18034]; Alignment" XX SQ Sequence 1100 BP; 226 A; 329 C; 346 G; 199 T; 0 other; aaataaataa ataaataggc cgtgcgcagt ggctcacgac tgtaattcca acattttaga 60 aggcggaggc cagcggatca cctgaggtca ggagttcggg accagcctga ccaacgtggt 120 gaaaccccca actctactaa aaatacataa attaggcggg cgtggtggtg gccgcctgta 180 atcccagcta ctcggtaggc tgcagcagga gaatggtttg aacccgggag gcagaggttg 240 cagtgagcca aaatcccctc actgcattcc agcctgagac taaaaaaaag aggcgatttc 300 ccacatcggt ggaaatttga gctgtttaaa ctctggatgc ctttttcagt tctaatattc 360 cagatctcct tggtggataa acacttcatt tcccttctcc tgagcagagc tcctgagccc 420 tggcccgctg ggaacctgtc acttctaaaa aagttcgagg tccggactgt ctctcccgga 480 gccttgaggc tgatgagacg gagcgagaga ggggccgggg ccgaatggag tctactcgcg 540 ggcccaggga ggccgccaga gggcgcccgg gaccgaccgc aagaataact tccttcctct 600 tccgctaact tcccggcagc gcgccgctca gggtgggggc cccgagggct ggggccgtcg 660 gcttccccct ggggatcccc cgcttcagag aaagccaagc gttaggcgca gccaaagccg 720 agaggcagcg gaagctcccg gcccggggtg gcgctgggtc agcgggtacc ttctcggcgg 780 tcccctggcc ggccgaactc gcgcctggtg tcctgtcacc ccgctccccg ccctgagtga 840 gcctgtcccc tctcaggggc gcgcccgagt cgctccgggt tggctgcgcc agtccagagt 900 taaactttca gccaatgaaa aagggcgcga ggcgtgacgc acggaaacgt catgggaatt 960 cccccctccg gggggccgag aaggggcttt cccggccctg agccctgctg gcaggcgagg 1020 tgtcgcgacc ggtcccaggt gggtcgggcg cggagagaag ccgcaaccag agccgccgcc 1080 acggtgagtg gctggattca 1100 // ID HSA_4792_NFKBIA standard; DNA; HUM; 1100 BP. XX AC 4792; XX DT 05-Sep-2005 (Created) XX DE NFKBIA: nuclear factor of kappa light polypeptide gene enhancer in DE B-cells inhibitor, alpha XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.14 34943607..34944706 (REVERSE) CC Score Points: 65 (97.0%) CC Chromosomal Location: 14q13 XX CC Database Reference HGNC: 7797; NFKBIA CC Database Reference ENTREZGENE: 4792 CC Database Reference UNIGENE: Hs.81328 CC Database Reference ENSEMBL: ENSG00000100906 CC Database Reference REFSEQ: NM_020529 CC Database Reference REFSEQ: NP_065390 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201502_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201502_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201502_s_at CC Database Reference TRANSFAC GENE: G002981; IkappaBalpha XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="14" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 34943607..34944706" FT /note="Genomic Strand: REVERSE" FT misc_feature 332..>1100 FT /note="ChIP-on-Chip Fragment: HNF6_hep" FT /note="PubMed:14988562" FT prim_transcript 999..>999 FT /db_xref="dbTSS:HSI02785" FT /note="Number of reported TSSs: 3" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:Zrv61971.seq" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP73215" FT prim_transcript 1004..>1004 FT /db_xref="ENSEMBL:ENST00000216797" FT prim_transcript 1006..>1006 FT /db_xref="dbTSS:SPL08518" XX SQ Sequence 1100 BP; 261 A; 334 C; 282 G; 223 T; 0 other; taaggcacta actaaactca ttcttcagcc tccttctcta agttctcctc gaatttgggt 60 gcccagaagt aggctcacga tcctttttct gcgggagcac aatgtaggtc agatagcata 120 aacgaatagc tacttatgaa cacaatagct actctgctat tgcaaggtat ccacaaccac 180 cactacaaac attaacacct tgctttactt gggaaacaaa aaaaatcatg gtcctattca 240 gcagtttccc catacaggga gcgtttgccc ctcccccagt caacagggct gttcatccct 300 aggaagtgat ttgagagttc tccaaggatt taggcttttc actcctccaa agctttcaca 360 acttctacct ggcgggggtg cgtggggggg tgggggcgaa gctaaaagtt cctttgctgc 420 aaagagcctg gtataggcag aaacaccggc gcggcctgca gccccctaac cacagtgcgt 480 ccttcccctt agaagtctgg ggaaagcaaa tccctacgcc cagccatcat ttccactctt 540 gcgttttcaa aagatcaaaa aacggaaagg accggcaggt tggcaaaccc caaagaggga 600 ccgcccatca ggtcggcgtc cttgggatct cagcagccga cgaccccaat tcaaatcgat 660 cgtgggaaac cccagggaaa gaaggctcac ttgcagaggg acaggattac agggtgcagg 720 ctgcagggaa gtaccggggg gagggggcct ggtcggaagg actttccagc cactcggcgc 780 tcatcaaaaa gttccctgtc cgtgacccta gtggctcatc gcagggagtt tctccgatga 840 accccagctc agggtttagg cttctttttc cccctagcag aggacgaagc cagttctctt 900 tttctggtct gactggcttg gaaattcccc gagcctgacc ccgccccaga gaaatcccca 960 gccagcgttt atagggcgcc gcggcggcgc tgcagagccc acagcagtcc gtgccgccgt 1020 cccgcccgcc agcgccccag cgaggaagca gcgcgcagcc cgcggcccag cgcacccgca 1080 gcagcgcccg cagctcgtcc 1100 // ID HSA_4794_NFKBIE standard; DNA; HUM; 1100 BP. XX AC 4794; XX DT 05-Sep-2005 (Created) XX DE NFKBIE: nuclear factor of kappa light polypeptide gene enhancer in DE B-cells inhibitor, epsilon XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 44341230..44342329 (REVERSE) CC Score Points: 3 (75.0%) CC Chromosomal Location: 6p21.1 XX CC Database Reference HGNC: 7799; NFKBIE CC Database Reference ENTREZGENE: 4794 CC Database Reference UNIGENE: Hs.458276 CC Database Reference ENSEMBL: ENSG00000146232 CC Database Reference REFSEQ: NM_004556 CC Database Reference REFSEQ: NP_004547 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38276_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203927_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:53701_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203927_at CC Database Reference TRANSFAC GENE: G003378; NFKBIE XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 44341230..44342329" FT /note="Genomic Strand: REVERSE" FT prim_transcript 827..>827 FT /db_xref="ENSEMBL:ENST00000275015" FT prim_transcript 987..>987 FT /db_xref="dbTSS:CBR03861" XX SQ Sequence 1100 BP; 313 A; 273 C; 317 G; 197 T; 0 other; gggacctgag cagagtgcaa cccagcatgt ctggggcctc cccaacctga ccccacttcc 60 ttgactgctg gggttgacca gaaactgtaa ctacccaagg ccagggtttc accctttgag 120 gaagaagaaa ctccacaacc actttacttt ttagacaaca gtttccctga gaagacgctc 180 tttccaaaaa aacattttca tgcccaattc catgtgatgt gggacgttga cacaggagac 240 tgtcttccag gacccaggag aactgctcct ttaaagataa tgggagtccc ctttccctac 300 ccgtacccct gggcactgat agggaaagat gagaaagcaa gagaaattga gataaatggg 360 caggggatag gaagcagtgc ttccccatcc catcgcctac atgccctccc ccaaagatgc 420 cagcttgtac ggacaattaa tagatatttc ttttaaaaca aatgaatgat ccgggaccgg 480 tggctcacag cctgtaatcc cagcactttg gtagtccgag gcaggcagat cgcttgaacc 540 caggagttcg agaccagcct gggcaacgta gcgagacccc cgtctctact tgtagtccca 600 gctactcgaa aggctgaggc aggagaatcg cttgaaccca ggaggcggag gttgcagtga 660 gcagagatca accactgcac tccagcctgg gcaacagagc aagacttcgt ctcaaaaaaa 720 taaaaaataa aaataaaaca aatgaattaa gaaatagaag tgaaagaagg aaacagtaca 780 tgcgtggaac taatgaatgg agtgaaggag gaagggggaa agagtgaatg aatgaatgaa 840 tgaatgagtg aatgaatcaa cgaaggagtg agtcaaggcc cgggaaccac agactccaag 900 cctacgcaga gcccgggaag ggggattccg gaggggcggg gcctctttcc ggaagcgccc 960 gccgggggcg gggagggggc ggggccatcc gcgtgaggcg accctgttgg tccggagggg 1020 cggggcgagg aggaggaccc gcttgggcgg ttcggctgcc cacagtaacc gctgggtgga 1080 cctggccagc gctccgaacc 1100 // ID HSA_5209_1_PFKFB3 standard; DNA; HUM; 1100 BP. XX AC 5209_1; XX DT 05-Sep-2005 (Created) XX DE PFKFB3: 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.10 6225900..6226999 (FORWARD) CC Score Points: 3 (13.0%) CC Chromosomal Location: 10p14-p15 XX CC Database Reference HGNC: 8874; PFKFB3 CC Database Reference ENTREZGENE: 5209 CC Database Reference UNIGENE: Hs.195471 CC Database Reference ENSEMBL: ENSG00000170525 CC Database Reference REFSEQ: NP_004557 CC Database Reference REFSEQ: NM_004566 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202464_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202464_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202464_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37110_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37111_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39522_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:56246_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="10" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 6225900..6226999" FT /note="Genomic Strand: FORWARD" FT prim_transcript 988..>988 FT /db_xref="ENSEMBL:ENST00000360521" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:HKR01595" FT prim_transcript 1012..>1012 FT /db_xref="dbTSS:HPR05394" XX SQ Sequence 1100 BP; 237 A; 333 C; 342 G; 188 T; 0 other; acactaataa gcacataggg agtcggtcag gcggtgaccc gtgcggtgga gagaaggcag 60 ccggcgggac gtggaagggt cgaggttaaa ccgaggtagt ggggaggccc ccagtgaaag 120 acgcgagttt ccggggtgct ccctctagcc agcagttaat tgcaattctg ccgggcgcgg 180 tggctcacgc ctgtaatccc agcactttgc gaggccgagg tgggcagatc actttaaacc 240 aggagttccc gaccagcctg ggcaacatga caatacccgt ttctacaaaa acatttagaa 300 aaattatctg ggcgtggtgg cgcacgcctg taatcccagc tacttgggag gctgaagcag 360 gagtatgggt tgagcctggg gaggtggagg ctgcagtgag ctatgatcgc accgctgcac 420 tccagcctgg gcgacagagt gagatcctgt ctcaaaacac acacacacac acacacacac 480 cccccaaaac aacaaacaaa aaaaaaaaag agaaagaaaa aattacacaa tttcagtttg 540 ttcaatttga gtcagctggt gattcgagcg tgtcccctgt gcccgtagga cataaaagta 600 aaaataagat ggaattccct caggtctcgt ccttcgggaa ggatggctcg gaacagcccg 660 aaagagaaaa gggagttggt ttcttcccgg accagttttc ccctgtcccg tggagtccac 720 aagacaggcg gcagcttcaa ggccggcaag ttccgcgtct ggggggctgc gggccgcccc 780 tgcgggaccg gggggatctg ggcgggacag ggcggcccgg cccacgcccc ggcttccccc 840 agcagcccga gggcgcccgg agctcacggc tggcgccgcc ccgcgcttcc tgcctcgccg 900 cggatcctcc tccgcgccgt gacgcgccag gctttgacca aatatgtccc tttcccctcc 960 ctcgcccgcc ccgccgcccg caggcgcccc gagtcgcggg gctgccgctt ggacgtcgtc 1020 ctgtctgggt gtcgcgggcc ggccccgcgg ggagcgcccc cggcgcgatg cccttcagga 1080 aaggtaggag tcccggtgac 1100 // ID HSA_5328_1_PLAU standard; DNA; HUM; 1100 BP. XX AC 5328_1; XX DT 05-Sep-2005 (Created) XX DE PLAU: plasminogen activator, urokinase XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.10 75339895..75340994 (FORWARD) CC Score Points: 63 (94.0%) CC Chromosomal Location: 10q24 XX CC Database Reference HGNC: 9052; PLAU CC Database Reference ENTREZGENE: 5328 CC Database Reference UNIGENE: Hs.77274 CC Database Reference ENSEMBL: ENSG00000122861 CC Database Reference REFSEQ: NM_002658 CC Database Reference REFSEQ: NP_002649 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211668_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205479_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205479_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211668_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37310_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205479_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211668_s_at CC Database Reference TRANSFAC GENE: G000415; uPA XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="10" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 75339895..75340994" FT /note="Genomic Strand: FORWARD" FT prim_transcript 999..>999 FT /db_xref="dbTSS:TIR06153" FT prim_transcript 1000..>1000 FT /db_xref="EPD:EP14054" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:TIR05974" FT /note="Number of reported TSSs: 9" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:T3R04980" FT /note="Number of reported TSSs: 2" FT prim_transcript 1028..>1028 FT /db_xref="ENSEMBL:ENST00000242464" XX SQ Sequence 1100 BP; 250 A; 316 C; 295 G; 239 T; 0 other; agagtgtaaa aggacaaaca gtgaaaaata aatcttcctc ttattttgtc ctccagtctc 60 ccaattcctc tactcagagg tgagaacaga acttccacac cctccagaac ctccacagtt 120 agaactgtct acatgtttcc attgtcttta cttttattct tgcctgcaca aataaatgaa 180 ttgctcatta tggaaacttc ccaaaagacc cgttaacact tcaataggaa gcaccaacag 240 tttatgccct aggactttgt tcccacaatc ctgtaacatc atatcacgac acctaaccca 300 atccttatca agccctgtca aaaacggact ttaaaccaag ctgcaaattt tcagtaatct 360 ggccttgcct ttccccctct gatagcacca tcaaacaaac ccccttactg ccgaaagcaa 420 taagcccggc tttgttccat ccactggttg tgttggtgat atctggggac tgccactgaa 480 cagacgcaca gagggagccc ctacaggcag gggtttttct gtctgtgctt ctgggagagt 540 atgtctcgta catttgtcgc gttgatgaag acttcacagc tccatcagct gcgggcaagg 600 gggtctgagg cagtcttagg caagttgggg cccagcgggg agaagttgca gaagaactga 660 ttagaggacc ccaggaggct tcagagctgg gcgaggtaga gagtctcctg tgcgccttct 720 ctcctctctg caattcgggg actccttgca ctggggcagg cccccggcca ggtgcatggg 780 aggaagcacg gagaatttac aagcctctcg attcctcagt ccagacgctg ttgggtcccc 840 tccgctggag atcgcgcttc ccccaaatct ttgtgagcgt tgcggaagca cgcggggtcc 900 gggtcgctga gcgctgcaag acaggggagg gagccgggcg ggagagggag gggcggcgcc 960 ggggcgggcc ctgatataga gcaggcgccg cgggtcgcag cacagtgcgg agaccgcagc 1020 cccggagccc gggccagggt ccacctgtcc ccgcagcgcc ggctcgcgcc ctcctgccgc 1080 agccaccggt gagtgccgcg 1100 // ID HSA_5366_PMAIP1 standard; DNA; HUM; 1100 BP. XX AC 5366; XX DT 05-Sep-2005 (Created) XX DE PMAIP1: phorbol-12-myristate-13-acetate-induced protein 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.18 55717208..55718307 (FORWARD) CC Score Points: 58 (98.3%) CC Chromosomal Location: 18q21.32 XX CC Database Reference HGNC: 9108; PMAIP1 CC Database Reference ENTREZGENE: 5366 CC Database Reference UNIGENE: Hs.96 CC Database Reference ENSEMBL: ENSG00000141682 CC Database Reference REFSEQ: NP_066950 CC Database Reference REFSEQ: NM_021127 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204286_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204286_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204285_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204285_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41048_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204285_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204286_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="18" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 55717208..55718307" FT /note="Genomic Strand: FORWARD" FT misc_feature 251..1099 FT /note="ChIP-on-Chip Fragment: HNF6_panc" FT /note="PubMed:14988562" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:DAT09185" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP74612" FT prim_transcript 1010..>1010 FT /db_xref="ENSEMBL:ENST00000316660" FT prim_transcript 1017..>1017 FT /db_xref="ENSEMBL:ENST00000269518" XX SQ Sequence 1100 BP; 212 A; 359 C; 259 G; 270 T; 0 other; gttcggaatc agggcagtgc tctctgccta agtgaacttg ggcaattttc tacaaacctc 60 agtttctgca cccgtaaagt agcaacggtt gttctgagga cggaatgaga aaatgcatgt 120 caaagtcctt agcatgaagc ggctctcagt aaccgttaac cactcctaat tactcctctt 180 cataatagta gaattactca tggcctcgcc aaacattatg caaataattt cacgttccca 240 ggtagctcag ccctcccaca aaagatttga acgttttcca tatgataacg atccactcgt 300 ttttgctaaa catccacaat gggcgatatc gacctatctg gaaggacaca cacaaatccc 360 ttcccaactc aaacacgatg ttctttctgg ctggcaccag ggcttctgtt tgcagtgact 420 tcctgggacc cggagctttc tcacagggcc tctggcatct cctctgcggt gattaaggtt 480 cttctcattt cccttccctg ttactgccca tactcttcaa gttcgaaaag tttccttttc 540 caatctcttt tctgggcttg tttacccaag tctctaattg ccaaggcctc tggtctctcc 600 ccacccacaa cgttcctcct ggttaaaccc ttcccctccc gccactccca gctcccgcca 660 ctcccagctc ccgccaccac tgccgctgac gacgtccagc gtttgcagat ggtcaaagcc 720 gacccccttc tcctcccacc tcgttttgta aggaagtaat ttcggggccg agcgctctgc 780 gccccccgcc gcgggtcggc gccgccgcgg gtcgggagcg tgtccgggca ggtcgcgctc 840 agcggggtac ttccccgccc gcgtcccgcg tccgctccca taacgccgtc tgcggggcgg 900 ggacaggggc ggggacaggg gcgggccggg cgtctagttt ccctacgtca ccagggaagt 960 tctcactgga caaaagcgtg gtctctggcg cggggatctc agagtttccc gggcactcac 1020 cgtgtgtagt tggcatctcc gcgcgtccgg acacccgatc ccagcatccc tgcctgcagg 1080 actgttcgtg ttcagctcgc 1100 // ID HSA_54434_SSH1 standard; DNA; HUM; 1100 BP. XX AC 54434; XX DT 07-Sep-2005 (Created) XX DE SSH1: slingshot homolog 1 (Drosophila) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.12 107753695..107754794 (REVERSE) CC Score Points: 3 (37.5%) CC Chromosomal Location: 12q24.11 XX CC Database Reference HGNC: 30579; SSH1 CC Database Reference ENTREZGENE: 54434 CC Database Reference UNIGENE: Hs.199763 CC Database Reference ENSEMBL: ENSG00000084112 CC Database Reference REFSEQ: NM_018984 CC Database Reference REFSEQ: NP_061857 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34082_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:57654_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1554274_a_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:221753_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1555624_a_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:221753_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:80528_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:221753_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="12" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 107753695..107754794" FT /note="Genomic Strand: REVERSE" FT prim_transcript 970..>970 FT /db_xref="dbTSS:TIR02530" FT prim_transcript 978..>978 FT /db_xref="ENSEMBL:ENST00000326495" FT prim_transcript 1057..>1057 FT /db_xref="ENSEMBL:ENST00000360239" XX SQ Sequence 1100 BP; 163 A; 371 C; 341 G; 225 T; 0 other; tcctgcttca gggcacgctg atcccccctg cttggagagc tgtctctctg ttctttcacc 60 tgttaatcct gcttatgctc aagcccaagc ctcagaataa agctcttctg ggaagccttc 120 cctgacctcc aaggagttgg ctgggtttca gaacacccag aaagaattca ttgaaaaaga 180 ttagcaaaat acttttttaa aaacgtgcct aataacttga ttaacctctg caaaatcagg 240 cgaatctatt ttgcttactg tttttgtttt ttgttttttg tttttttgag accgagtctc 300 gctctgtcgc ccaggctgga gtgcagtggc gcgatctcag ctcattgcaa cctccgcctc 360 ccagattcaa gcgattctct tgcctcagcc tcccgagtag ctgggactac aggcgcgcac 420 cactgcgccc agctaatttt tgtcttttta gtagagacgg ggtttcacca tgttggccag 480 gatggtctcg atctcttgac ctcgtaatcc gcccgcctca gcctcccaaa gtgctgggat 540 tacaggcgtg agccaccgcg cccggcccca ggacgtcttt tatttcctgg tcgctgtaca 600 gtcctgtctg cacggtcgcc gggcctcagt ttccccaggc agagcagcgg gcagggcccc 660 tggggcgtac gggctccggg cggcgcgcgc gcccccgagt cccaggcctg atagcggggc 720 gcgcgggcgg gggcgcgtgt gtcgggcgcg cgagggacgt gatcgaccag ccgaggcctc 780 gggcagccct cagggccccc gcgcacgcgc gcctcctcgt cccgccctgc ccgcttcccc 840 gcccactccg cgcactgagg cctgcgcgcg ccggcgcggg aggcgggagc tgggggcggg 900 ggcggtggcg acgccgaggg ggaggggcgg gcccggcccg gctcggcccg gccgcccgcg 960 cgcggctcca ggaggccccg ggcccggccc gggcggcggt ggcggtggcg gctctagctc 1020 gagacgtctg tggcgccctc gcaccgcgcc gcagccatgg ccctggtgac cctgcagcgc 1080 tcgcccacgc ccagcgccgc 1100 // ID HSA_56892_C8orf4 standard; DNA; HUM; 1100 BP. XX AC 56892; XX DT 07-Sep-2005 (Created) XX DE C8orf4: chromosome 8 open reading frame 4 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 40129162..40130261 (FORWARD) CC Score Points: 6 (100.0%) CC Chromosomal Location: 8p11.2 XX CC Database Reference HGNC: 1357; C8orf4 CC Database Reference ENTREZGENE: 56892 CC Database Reference UNIGENE: Hs.283683 CC Database Reference ENSEMBL: ENSG00000176907 CC Database Reference REFSEQ: NP_064515 CC Database Reference REFSEQ: NM_020130 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:218541_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:218541_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:218541_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:65854_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 40129162..40130261" FT /note="Genomic Strand: FORWARD" FT misc_feature 261..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF6_panc" FT /note="PubMed:14988562" FT prim_transcript 983..>983 FT /db_xref="ENSEMBL:ENST00000315792" FT prim_transcript 985..>985 FT /db_xref="dbTSS:PNC05769" FT prim_transcript 997..>997 FT /db_xref="dbTSS:RCT07445" FT /note="Number of reported TSSs: 2" FT prim_transcript 999..>999 FT /db_xref="dbTSS:UBA04035" FT prim_transcript 1044..>1044 FT /db_xref="dbTSS:HSI11036" FT misc_feature 1048 FT /note="SECONDARY ANCHOR: MMU [69068]; Alignment" XX SQ Sequence 1100 BP; 315 A; 245 C; 213 G; 327 T; 0 other; agaaaaacga aaagacctgt cctgctttct taaaggacta gaaagcggac caggcgtaag 60 atccacaaag agaatctcca ggaccctttg aagctcacat ttagcatatg acaactccat 120 aggtcagtga ggacactggc tggcttgaat attgtggaag acaggaagaa cacatttata 180 tgcttccaaa gaagttattg ctctatgtct gggtaatgcc aaaataaatt tgaaaacaaa 240 agatcacctc gttcattttg ggcactgtgc acgtaaaaca cttgattaac ttttcctgct 300 ggcttttttg atagctattg ttgtggatgt atacacaagc ctaaggagat agcctctact 360 attcatatta ttactacacc caaattacaa tggtcttcag tgacacttag cacttgtaca 420 caatctctga aaagtcaccg tttcaagctg tgtcatgtca gcgttttgta tgtaaaatcc 480 catcctagaa ttgatcacac cccaaattat tatccttgat tgctcagctt tctctcagta 540 gctctggagt tgcccctgat atggatgtcc aaagggcact gatgtggact gccaaatgtt 600 tgcagtgcac tttaattact tctctgcgaa cgaaagcttt cctgtagtta gcagaacccc 660 ttgttctaac tgtcgtttgg gaagatttga gagtctaagc aacctcgttt atgtcttatc 720 tttgcatttt cctgtattca gctattttct taaaggaagg cccaggtctg tattatccta 780 ctgccacata ggaagtaaaa tgagtactca cagccttgcg cctaatcact gaacacagct 840 tttagtaatg ttttacacaa gaacaggata ttggcaactc aactgttaag cctttctgtg 900 attattcttc cttgagatca ctctgatgtc accagtgtaa tttgagcctg gagcttttgt 960 tcacacttta aatagcagtc ccagaatgat ttcactacag actctctgga aagcctggga 1020 gctgaattcc ggaagatccc cacatcgatg aaagcaaagc gaagccacca agccgtcatc 1080 atgtccacgt cgctacgagt 1100 // ID HSA_57007_CMKOR1 standard; DNA; HUM; 1100 BP. XX AC 57007; XX DT 07-Sep-2005 (Created) XX DE CMKOR1: chemokine orphan receptor 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 237259443..237260542 (FORWARD) CC Score Points: 1 (100.0%) CC Chromosomal Location: 2q37.3 XX CC Database Reference HGNC: 23692; CMKOR1 CC Database Reference ENTREZGENE: 57007 CC Database Reference UNIGENE: Hs.471751 CC Database Reference ENSEMBL: ENSG00000144476 CC Database Reference REFSEQ: NP_064707 CC Database Reference REFSEQ: NM_020311 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212977_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212977_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212977_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34288_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="2" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 237259443..237260542" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000272928" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [12778]; Alignment" FT misc_feature 1025 FT /note="SECONDARY ANCHOR: MMU [12778]; Alignment" FT misc_feature 1048 FT /note="SECONDARY ANCHOR: RNO [84348]; Alignment" XX SQ Sequence 1100 BP; 304 A; 207 C; 286 G; 303 T; 0 other; tctcgaaaag ttttagctct ggagaaggcg tgaatacagc tggtgccttc atacactcca 60 cttgagccgc tctttaagaa ctccaggaga tcagaaagca atacgaaagc cagagcattg 120 cacatgggat gggctggcgg gtggcctttg ggtccctatc ttatggacga tttttgtaaa 180 tggggcattg gagatgagta tcacctggat cacattttta ggttgaattc ctccgtgggg 240 ggaactttag caatacgcat ccaaataaga atgtagattg caataattgt agtaaagtgt 300 ttgccagact catctcagaa aaagacatta tcaaaaggca tttattatct tcctaatgcg 360 tgtctggcac tgggcagaca ctgtagaata ctatcttgat tagagtctca aggattttgt 420 acttaaagtc ctttacaaat aaaagtattc aagtataatc tattataaag actcttttct 480 ccactttggg gatatacggt gtggcatcga ttcattggtc ataccaaaac tgttacttct 540 gttttggagg aattaacaag gaaaacccag gcttagtaaa tcaacatcga agttcagaag 600 ttcagagtaa tttgtcttgg gaacaaagtc ctccctagag cgaagaggca ttcacaggag 660 ctcttggtgt taatgggatt attcaagata tacctgagac cagataaata tttgatgatt 720 ttgccaagca ctagggtttc tttgcagttt gtctttggct gacgttttcc ccccgtgggg 780 tttggacttt gtggcttcac cagattttgc aaatgaaaga aggctggggt ttcccaagag 840 tacacttgtg caggaaacaa cagactagtg aggtttacaa gaggggggtg tgtgtgtgtg 900 tgtgtctgcc tgtgggatgg gggtggcacg ggggagagag agatgtgggt tacaaagctg 960 ccatctagag gctagaggct cctttctgca gtgtatataa tgcaagtctg cagccagcag 1020 agctcacagt tgttgcaaag tgctcagcac taagggagcc agcgcacagc acagccagga 1080 aggcgagcga gcccagccag 1100 // ID HSA_5743_PTGS2 standard; DNA; HUM; 1100 BP. XX AC 5743; XX DT 06-Sep-2005 (Created) XX DE PTGS2: prostaglandin-endoperoxide synthase 2 (prostaglandin G/H DE synthase and cyclooxygenase) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 183381112..183382211 (REVERSE) CC Score Points: 7 (41.2%) CC Chromosomal Location: 1q25.2-q25.3 XX CC Database Reference HGNC: 9605; PTGS2 CC Database Reference ENTREZGENE: 5743 CC Database Reference UNIGENE: Hs.196384 CC Database Reference ENSEMBL: ENSG00000073756 CC Database Reference REFSEQ: NP_000954 CC Database Reference REFSEQ: NM_000963 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1554997_a_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1069_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204748_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204748_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204748_at CC Database Reference TRANSFAC GENE: G001237; PES2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 183381112..183382211" FT /note="Genomic Strand: REVERSE" FT misc_signal 859..883 FT /note="TRANSFAC Site R08091" FT misc_signal 882..912 FT /note="TRANSFAC Site R14626" FT misc_signal 917..941 FT /note="TRANSFAC Site R14627" FT misc_signal 930..956 FT /note="TRANSFAC Site R08092" FT prim_transcript 999..>999 FT /db_xref="ENSEMBL:ENST00000186982" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:SMR09283" FT /note="Number of reported TSSs: 5" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [19225]; Alignment" FT /note="PRIMARY ANCHOR: RNO [29527]; Alignment" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:SMR04184" XX SQ Sequence 1100 BP; 295 A; 275 C; 278 G; 252 T; 0 other; ttaccagtat ctcctatgaa gggctagtaa ccaaaataat ccacgcatca gggagagaaa 60 tgccttaagg catacgtttt ggacatttag cgtccctgca aattctggcc atcgccgctt 120 cctttgtcca tcagaaggca ggaaacttta tattggtgac ccgtggagct cacattaact 180 atttacaggg taactgctta ggaccagtat tatgaggaga atttaccttt cccgcctctc 240 tttccaagaa acaaggaggg ggtgaaggta cggagaacag tatttcttct gttgaaagca 300 acttagctac aaagataaat tacagctatg tacactgaag gtagctattt cattccacaa 360 aataagagtt ttttaaaaag ctatgtatgt atgtgctgca tatagagcag atatacagcc 420 tattaagcgt cgtcactaaa acataaaaca tgtcagcctt tcttaacctt actcgcccca 480 gtctgtcccg acgtgacttc ctcgaccctc taaagacgta cagaccagac acggcggcgg 540 cggcgggaga ggggattccc tgcgcccccg gacctcaggg ccgctcagat tcctggagag 600 gaagccaagt gtccttctgc cctcccccgg tatcccatcc aaggcgatca gtccagaact 660 ggctctcgga agcgctcggg caaagactgc gaagaagaaa agacatctgg cggaaacctg 720 tgcgcctggg gcggtggaac tcggggagga gagggaggga tcagacagga gagtggggac 780 taccccctct gctcccaaat tggggcagct tcctgggttt ccgattttct catttccgtg 840 ggtaaaaaac cctgccccca ccgggcttac gcaatttttt taaggggaga ggagggaaaa 900 atttgtgggg ggtacgaaaa ggcggaaaga aacagtcatt tcgtcacatg ggcttggttt 960 tcagtcttat aaaaaggaag gttctctcgg ttagcgacca attgtcatac gacttgcagt 1020 gagcgtcagg agcacgtcca ggaactcctc agcagcgcct ccttcagctc cacagccaga 1080 cgccctcaga cagcaaagcc 1100 // ID HSA_58472_SQRDL standard; DNA; HUM; 1100 BP. XX AC 58472; XX DT 07-Sep-2005 (Created) XX DE SQRDL: sulfide quinone reductase-like (yeast) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.15 43713550..43714649 (FORWARD) CC Score Points: 86 (96.6%) CC Chromosomal Location: 15q15 XX CC Database Reference HGNC: 20390; SQRDL CC Database Reference ENTREZGENE: 58472 CC Database Reference UNIGENE: Hs.511251 CC Database Reference ENSEMBL: ENSG00000137767 CC Database Reference REFSEQ: NM_021199 CC Database Reference REFSEQ: NP_067022 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:217995_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:46305_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:217995_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:217995_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="15" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 43713550..43714649" FT /note="Genomic Strand: FORWARD" FT prim_transcript 712..>712 FT /db_xref="dbTSS:HRT02368" FT misc_feature 866..>1100 FT /note="ChIP-on-Chip Fragment: cMyc" FT /note="PubMed:14980218" FT prim_transcript 941..>941 FT /db_xref="dbTSS:LNF03356" FT prim_transcript 970..>970 FT /db_xref="dbTSS:HSI00178" FT /note="Number of reported TSSs: 3" FT prim_transcript 973..>973 FT /db_xref="dbTSS:REC00676" FT prim_transcript 974..>974 FT /db_xref="dbTSS:SLV02117" FT /note="Number of reported TSSs: 2" FT prim_transcript 978..>978 FT /db_xref="dbTSS:WMD01457" FT prim_transcript 982..>982 FT /db_xref="dbTSS:adKA01523" FT prim_transcript 988..>988 FT /db_xref="dbTSS:HRC01433" FT prim_transcript 989..>989 FT /db_xref="dbTSS:HSI05441" FT /note="Number of reported TSSs: 4" FT prim_transcript 991..>991 FT /db_xref="dbTSS:HSI07323" FT prim_transcript 993..>993 FT /db_xref="dbTSS:MPB04968" FT prim_transcript 995..>995 FT /db_xref="ENSEMBL:ENST00000260324" FT prim_transcript 996..>996 FT /db_xref="dbTSS:HSI11343" FT /note="Number of reported TSSs: 2" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:HRC03088" FT /note="Number of reported TSSs: 2" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:HSI08679" FT /note="Number of reported TSSs: 3" FT prim_transcript 1005..>1005 FT /db_xref="dbTSS:HSI05863" FT /note="Number of reported TSSs: 2" FT prim_transcript 1006..>1006 FT /db_xref="dbTSS:SMR05751" FT prim_transcript 1009..>1009 FT /db_xref="EPD:EP73223" FT prim_transcript 1012..>1012 FT /db_xref="dbTSS:MPB07189" XX SQ Sequence 1100 BP; 243 A; 305 C; 316 G; 236 T; 0 other; cagctactca ggaggctgag acaccagaat tggttgaacc catgaggcag atgttgcagt 60 gagccgagat tgctctactc actgcgctcc agcctgggca acacagtgag actctgtttc 120 aaaaaacaac aacaacaact atatatatat atatatatat atatattcaa aattcataaa 180 accaaataag tgtaaaagaa actcaaactt tcaagggttt atttttgttt gtttttttga 240 aagcttctag cacttgcact tctcaggtta tgagactttt gggacaccct gtatttattg 300 taaaaagggt tactgaatct gatatggtgg agaaccactc actgagactt tacatcaacc 360 tggaaagagc cgccaactga aaatgtccag tcatgaatat gggatgggac actgtggagg 420 ccagtggctg gaagccagct tacccctgcc tgcgcgtttt gaaggaaggg ctccagcgca 480 caccaaagct gaacctcggt caccttctct gtgaaatgag cgcgggaata cctgtgtttc 540 tgggcagctg tgtgaacccg gtgagaagcc cagggcacat aggaggaccc agtgggaaca 600 gccagagcct ctctgcacag cgccccgcct ccgcttttgc ctgccctgat tacaaaacgc 660 tgttggcacc caggggcgga agcgtcaggt ggcctcggtg tcctccgcct gtgcgcccca 720 gcctgcgggg ccgcccttca gggcgcgcaa ggggcgagtc tgtccagccg gcagcacccc 780 aggccggatg gacgcttgtt cctggttctg tgccccgtga gcgctcaacg ccctggtgtg 840 ttcactgacc atggtgcctg ggctgcggcg ccgggcgggg cacggcggga cttttcggga 900 cctttcctgg ggggagcctc gctttccccg cctccagcct ccgcccggat ggcaggcggg 960 cggggcccca gtccaggcct tgagacccag aagggagcga aggtttttgc tgcgccaacg 1020 cagtgaccga aggctccgct cacgcccggg taagaggcat ccgcggccga tctttggccc 1080 tgggccagcg gagggagact 1100 // ID HSA_5905_RANGAP1 standard; DNA; HUM; 1100 BP. XX AC 5905; XX DT 06-Sep-2005 (Created) XX DE RANGAP1: Ran GTPase activating protein 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.22 40023364..40024463 (REVERSE) CC Score Points: 1 (6.2%) CC Chromosomal Location: 22q13 XX CC Database Reference HGNC: 9854; RANGAP1 CC Database Reference ENTREZGENE: 5905 CC Database Reference UNIGENE: Hs.183800 CC Database Reference ENSEMBL: ENSG00000100401 CC Database Reference REFSEQ: NP_002874 CC Database Reference REFSEQ: NM_002883 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212125_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212127_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212127_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212125_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212127_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212125_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:1553535_a_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32151_at CC Database Reference TRANSFAC GENE: G005321; RANGAP1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="22" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 40023364..40024463" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000359514" XX SQ Sequence 1100 BP; 330 A; 270 C; 239 G; 261 T; 0 other; cggtgaaacc ccgtctctac taaaaataca aaaaattagc tgggcgtagt ggcgggagcc 60 tgtagtccca gctactcagg aggctgaggc aggagaatgg cgtgaacccg ggaggcggag 120 cttgcagtga gccaagatcg cgccactgca ctccagcctg ggcgacagag cgagactccg 180 tctcaaaaaa gtaaaataaa ataaaataaa ataaatgaaa agtaacttgc taaggtggcc 240 caggactctg ggaaagggtg acgatttgga gccagaaaac tgggtgggaa tcctacctct 300 gctgtctgac tttccagcaa gacacacaat tcggcctaag gtttcttatc tagaaaatgt 360 ctacctgaca cagttgctat ggaggacaga tgagccaaca catgtgaaag cccttttgtt 420 ataaactaaa aagtgatatt tgagggatta ttattttcag attgagggat tattttcaga 480 ttctctatcc atgtctcaac cgacatctca gctttcctac taagactcga gagatcagca 540 catcccacca agcttctaag ccccacaata atctaccaaa acccccattc ctgtctaacc 600 tatacaaaag ccagcagcta agaacacaca gcatctacag aacagaaact ttatcccagc 660 tcagggacaa caaagtctct ctcccatcct cagatctcat ccctcctgga caggttcttt 720 cttcccacct taagtctccc cacttctcaa acatgctcca tccaactgtt gaccaggtgt 780 catttccacc ttgcagtcca acttctgtgg gaggtggaca cggggaaaga agaccaccac 840 ggaggggatg gctgtatgtg tgtagaggaa gtattggtag tagaactaaa gattctgcca 900 gcattttgtg tccaacacag ttgctacatg tactataatt atctcatttg tgtgaaaatt 960 caaggatctg cattctgcta ttttcatcag gctgaactgc agatgctgag gaatatggca 1020 agaagttggg gttcaaagtc tgatgccaaa gctagcaacc cgagaaataa aaccgctgat 1080 caccagctcc ccactcaggc 1100 // ID HSA_597_BCL2A1 standard; DNA; HUM; 1100 BP. XX AC 597; XX DT 05-Sep-2005 (Created) XX DE BCL2A1: BCL2-related protein A1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.15 78050556..78051655 (REVERSE) CC Score Points: 3 (100.0%) CC Chromosomal Location: 15q24.3 XX CC Database Reference HGNC: 991; BCL2A1 CC Database Reference ENTREZGENE: 597 CC Database Reference UNIGENE: Hs.227817 CC Database Reference ENSEMBL: ENSG00000140379 CC Database Reference REFSEQ: NP_004040 CC Database Reference REFSEQ: NM_004049 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:2002_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205681_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205681_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205681_at CC Database Reference TRANSFAC GENE: G005817; BCL2A1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="15" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 78050556..78051655" FT /note="Genomic Strand: REVERSE" FT prim_transcript 958..>958 FT /db_xref="ENSEMBL:ENST00000267953" FT /note="Number of reported TSSs: 2" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [170929]; Alignment" FT prim_transcript 1090..>1090 FT /db_xref="ENSEMBL:ENST00000335661" XX SQ Sequence 1100 BP; 276 A; 262 C; 199 G; 363 T; 0 other; aacttccacc tctatctagc tgcaaaacat tttcttttct tttttttttt ggagacagag 60 tctcgctctg ttgcccagac tggagtgcag tggcgtgatc ttggctcact gcaacttctg 120 tctcccgggt tcaagcaatt ctcctgcctc agcctcccga gtagctggga ttacaggcac 180 acgccacccg cctggctaat tttttgtatt ttagtacaga cggggattta ccatattgcc 240 caggctggtc tcaaactcct gagctcaggc aatccgcccg ccttgtcctc ccaaagtgct 300 aggattacag gcgtgagcca acgcggccgg ccttgtaaaa cattttcatc acacaaaaga 360 aaaccttcta cccattaagc agttactcct tcctcttctc agcccctgtc aaccaccaat 420 ttgctttcta tcctatggat ttaactgtct ggatatttca tagaaataga atcacataat 480 gtatgacctt ttctgtttgg cttctttcta ttagcctaat gtttttgagg ttcattcctg 540 ttgaagcatg tatcagttct tcattccttt tttgggatga ataatgttcc ataatttatt 600 tatcctttcg tctgttgatg aacatttgag ttgtgtccac atcttggcta ttgtgaatag 660 tgctgccatg tacattcgta tgtaagtatt tgagtatctg ttgggtgtat acctatgaat 720 ggaattgctg ggtcttttga caattctgta tttaactttt tgagaaactg ccaacatttt 780 cacaggggtt gtaccatttc acattcccac cagcaatcta caaggattct aatttctcca 840 catcctgcat ttaagacttg caaagctgaa ttaatcacag gatgaggaag tggcttctct 900 gaaacatttt cctctttcac attttaaact ttctctttca tacatgacat gaaacacagc 960 ctacgcacga aagtgactag gaggaaggat attataaagt gatgcaaaca gaaattccac 1020 cagcctccat gtatcatcat gtgtcataac tcagtcaagc tcagtgagca ttctcagcac 1080 attgcctcaa cagcttcaag 1100 // ID HSA_5971_RELB standard; DNA; HUM; 1100 BP. XX AC 5971; XX DT 06-Sep-2005 (Created) XX DE RELB: v-rel reticuloendotheliosis viral oncogene homolog B, nuclear DE factor of kappa light polypeptide gene enhancer in B-cells 3 (avian) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.19 50195552..50196651 (FORWARD) CC Score Points: 1 (50.0%) CC Chromosomal Location: 19q13.31-q13.32 XX CC Database Reference HGNC: 9956; RELB CC Database Reference ENTREZGENE: 5971 CC Database Reference UNIGENE: Hs.307905 CC Database Reference ENSEMBL: ENSG00000104856 CC Database Reference REFSEQ: NM_006509 CC Database Reference REFSEQ: NP_006500 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205205_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205205_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:570_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205205_at CC Database Reference TRANSFAC GENE: G004623; RELB XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="19" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 50195552..50196651" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000221452" XX SQ Sequence 1100 BP; 217 A; 353 C; 295 G; 235 T; 0 other; tgccattcgc agactgaata actgagcttt tgagctcaaa gtggtctggg ctatttatgg 60 gtaactttca ggggctgcag ggaggaacaa accaataaat aaaacatcca tgcattcatc 120 caataaactt tttttttttt gagatgggag tctcgctctg ttgcccaggc tggagtgcag 180 tggcacgatc tcagctcact gcaacctccg cctcccaggt tcaagctatt ctcctgcctc 240 agcctccgga gtagctggca ttacaggcgc acaccaacac gcccagctaa tttttgtatt 300 tttagtagag atgggatttc accatgtcgg tcaggctggt ctcgaaatcc tgacctcgtg 360 atgtgcctgc ctcggcctcc caaagtgctg agattacagg catgaaccac cgcgcccggc 420 ctccaataaa catttattgg gcacctacgg tgttccaggc gctggtctag gcgttggggt 480 tacaacaacg cacaaaacat aaattctgaa gctgacacgc tagctttaaa cgttccttaa 540 atatcttcat cctcaattta cggttgagga aactgaggtg tagcgagacc ttggaggttt 600 ccgaaatatt attatggatg gcaggtgtag agccctgcca acctctcgat cctgaagctc 660 cccttccagc ctgagaaacg gcaggttcaa gtcccactgg gagaccaaag cggggagcgg 720 ctcagtttgc cggcttgctc aatgggtaag gcgtgatggc tctaagcagg cctcagttgt 780 ctcgtccaga gcaatgggca gcgacgcctg cccaacccct cctgagcgcc cagcctccct 840 ttcccggccg gccccgcccc cgcgatcacg tgacgcgtgg gggttttccc gttccccagg 900 cgtgacgtca cggcggggtg cagaccaatg ggcgcgcagg ccggcggcgc cggggaattc 960 cgccgccccg cccccgcccg ccgcccgccc ggcccggccc cgcgccccgc gcagccccgg 1020 gcgccgcgcg tcctgcccgg cctgcggccc cagcccttgc gccgctcgtc cgacccgcga 1080 tcgtccacca gaccgtgcct 1100 // ID HSA_602_BCL3 standard; DNA; HUM; 1100 BP. XX AC 602; XX DT 05-Sep-2005 (Created) XX DE BCL3: B-cell CLL/lymphoma 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.19 49942820..49943919 (FORWARD) CC Score Points: 1 (100.0%) CC Chromosomal Location: 19q13.1-q13.2 XX CC Database Reference HGNC: 998; BCL3 CC Database Reference ENTREZGENE: 602 CC Database Reference UNIGENE: Hs.31210 CC Database Reference ENSEMBL: ENSG00000069399 CC Database Reference REFSEQ: NP_005169 CC Database Reference REFSEQ: NM_005178 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204908_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204907_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204908_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204908_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204907_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1796_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204907_s_at CC Database Reference TRANSFAC GENE: G004492; Bcl3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="19" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 49942820..49943919" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000164227" XX SQ Sequence 1100 BP; 228 A; 372 C; 362 G; 138 T; 0 other; gcagcaccgg cctcggtcgc gctgactctg gcctggtgtc cgtgtctctt gctatctctc 60 tttctctcaa gatctctgcg cctgtctcca tgtctctttc tctctgtgca cctaggattt 120 tccgagcacc caccccggtg ccccgcgggc cccggctggg ggcagggccc ccaacgagtg 180 cagagacaca atcagtggag cgctccccac cctcacccca cccccagccc ctttagaccc 240 acagctgatg aggcacgtgg agtggcagag atggaagagg ggagggagag gaatcgttcc 300 tggccgcctg ccgagtgcca gtccctgccc cgggtgcgtc tcttcactcc cactaaggag 360 gaaacggctc agagagggga agtgtttggc caaggtcacc cagcgagtaa gtgggaaccg 420 agattccaaa ccccgtccca gagatgccaa ggcctcctga gagacagaga agcagacagc 480 aactgagagg cagagagatg gtgacagaca caaagagaca aaagagagag acagagacgg 540 aacagagcac acagagacaa acgcggggtt gcggagagaa acacctactc agacaggaga 600 accagagaga cagttacaga ctcagagata gagatgttga gagatagggc cagaaagaca 660 aaaacagagg cagagagagc ggcccttggc agcaggggtg gggacacccc cccacccccc 720 gaccccgcct cctctccccc cacccctcct ttcctctccc tcccccgccg aggcctggct 780 gccccaggcg ccgcgggccg ggagggggca agcggggcgc ggcgcgggcg gggcgcaggg 840 caggctgcac ctcagagcgg cgggagcagc ggcgggtcca ggaaacccct ggggcgtacg 900 ggtggccccg ggggggccgg gggcggggag gcgggcggcc ggcaccgccc cggccgacaa 960 aagtcccttc agttcagccg gctgcagggg aagtcccggc gcccggcgaa accaccctcc 1020 cgtgcagccg agcccagccg ctctccggcc gccgtccccg gcggccccat gccccgatgc 1080 cccgcggggg ccatggacga 1100 // ID HSA_6274_S100A3 standard; DNA; HUM; 1100 BP. XX AC 6274; XX DT 06-Sep-2005 (Created) XX DE S100A3: S100 calcium binding protein A3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 150334708..150335807 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 1q21 XX CC Database Reference HGNC: 10493; S100A3 CC Database Reference ENTREZGENE: 6274 CC Database Reference UNIGENE: Hs.433168 CC Database Reference ENSEMBL: ENSG00000188015 CC Database Reference REFSEQ: NP_002951 CC Database Reference REFSEQ: NM_002960 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206027_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39633_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206027_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206027_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 150334708..150335807" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000340845" XX SQ Sequence 1100 BP; 216 A; 303 C; 330 G; 251 T; 0 other; ccagactggc ctttgatgtg tgcgtggata ggtgggcagg tggggcctgt aatgggtctg 60 ctgagggatc cctgagggca tcctcagtgt tgacctactt gtgtccccca taattgcttc 120 cttcctttct tgggaggcta caaatagtga cgccctgtct ctaagctcct acagctgaaa 180 cgccagcacc agtggtgagt gccagctgct tgggtcctgc cctgggttga gtgtcagggc 240 agtttgggga cccccagtag ccagcctgac tcctgaccca gggtctggca ttggaagcag 300 agagatgacc acaggcgggc ctgacacggg gagggaagtc agatatagtg gacgcagagg 360 tttccttaca cagtgagggg ctgttgggga agtttgggca gggaggtgtg tagagctaag 420 gtctgccttg gggtgggagc actgggctca aggctctggt cttccccttg atcaggcccc 480 tcacctgctc cttgcctcct tgcttcacct ctgagtctcc tcatttctga ggatcatggc 540 cctttcctct cctgggaacc tggacacctt gctctaatcc tggggtgttt acaatgaatt 600 aaatcctggc agtgcttggc actccccact ccccttcccc tactttcctg ccagccacaa 660 ccatgccagc catttgctcc cagcaggggg cccagcagtg ggcaaatctt cagggagagt 720 cttggccctg gccgccctgt gctgcaggac tcttgtcccg tgggggaatc aggagtgagt 780 cactgggcta gcatggaaaa aactcttgcc ttcctggctg ccttcgggtt ttcccaggct 840 ggaggcatca tcccagaagg gcggtggaag gggacagtgg aagtgggggg aggtgagcaa 900 ttccaggaag ggcttcccct ccaatagaac agagtatccc tatacagaac ctccctgctc 960 aaaaccccca ggggtcggga gggtaacctc aggggaggcc agtctcagat tggtaaacac 1020 ccgaactggt caactctcaa gagaccatct ggttcaggtt cctgactggg ccagcgaggt 1080 gagatgaacc ccaacttaca 1100 // ID HSA_6303_SAT standard; DNA; HUM; 1100 BP. XX AC 6303; XX DT 06-Sep-2005 (Created) XX DE SAT: spermidine/spermine N1-acetyltransferase XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.X 23559948..23561047 (FORWARD) CC Score Points: 72 (96.0%) CC Chromosomal Location: Xp22.1 XX CC Database Reference HGNC: 10540; SAT CC Database Reference ENTREZGENE: 6303 CC Database Reference UNIGENE: Hs.28491 CC Database Reference ENSEMBL: ENSG00000130066 CC Database Reference REFSEQ: NM_002970 CC Database Reference REFSEQ: NP_002961 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213988_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210592_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203455_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213988_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203455_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210592_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213988_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34304_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203455_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210592_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="X" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 23559948..23561047" FT /note="Genomic Strand: FORWARD" FT misc_feature <1..580 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT prim_transcript 997..>997 FT /db_xref="dbTSS:RCT07790" FT prim_transcript 998..>998 FT /db_xref="dbTSS:KDN06206" FT /note="Number of reported TSSs: 11" FT prim_transcript 999..>999 FT /db_xref="dbTSS:DMC07911" FT /note="Number of reported TSSs: 2" FT prim_transcript 1000..>1000 FT /db_xref="EPD:EP73721" FT /db_xref="ENSEMBL:ENST00000252349" FT /note="Number of reported TSSs: 2" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:kaia5187.seq" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:PLR04337" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:KDN04495" FT prim_transcript 1028..>1028 FT /db_xref="dbTSS:KAT05025" FT /note="Number of reported TSSs: 2" FT prim_transcript 1029..>1029 FT /db_xref="dbTSS:ColF4218.seq" XX SQ Sequence 1100 BP; 324 A; 253 C; 269 G; 254 T; 0 other; aaactatgaa ataaaccctt caagaatttt aagatgggct ggtccaaagg tagtgagtta 60 tctcagttga ttgttcacaa tcagttacac atcaaactcc ttattttact ctgactactg 120 cacttgacta gtctaaaaaa agaattataa gatgaattaa agacacgttc agataagcaa 180 aactgagaac gtttggcaaa agcagatctt tactaaagga aattatgaag aatgtacctc 240 gggcagaagg aaaagtgtca agatcaagtg tcaaggaaga ttagagattt aagaaggtat 300 aagaaggtta gaaaagtaag aaaaaaatat gccgtcaact ctaaaaacta caagtataaa 360 gaaaaaagat tattgggaaa tccaaataac ctaccttagg aaattctaaa agaatatacg 420 agctcacatt cctttggtca taagagcagt gtcatcatta gacatcaggt cgcctctgga 480 aaattccatt gtgagtttaa aaggcaaatg acgtctataa ttctaaaact agttctccca 540 ccgaaactct agaaaggatc ttgggatctg cagggtctcc cggatcacac tttgagaact 600 gctgctttag tcttcctccc atctcctaag gccagagctc ctgagtttgc ttcccactgg 660 ccaaggagaa aagagcaagg tcacttgtcg gggggctgca gagggaatta ccttctttca 720 tttgcaaatg ttactggggg acacaccggc tcccagtagg gtttccgcca aggctccgcg 780 aaacgccact agagggcgcc gctagcgaat cccacagcgc gccccgctgc ccccactttt 840 gtcctccggg ttcacacggg cgcccggaag agagggtggt gcctgggaga ggaaacgatg 900 cgccccgggg ccgcggcctc attggatgag aggtcccacc tcacggcccg aggcggggct 960 tctttgcgct taaaagccga gccgggccaa tgttcaaatg cgcagctctt agtcgcgggc 1020 cgactggtgt ttatccgtca ctcgccgagg ttccttgggt catggtgcca gcctgactga 1080 gaagaggacg ctcccgggag 1100 // ID HSA_6347_CCL2 standard; DNA; HUM; 1100 BP. XX AC 6347; XX DT 05-Sep-2005 (Created) XX DE CCL2: chemokine (C-C motif) ligand 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.17 29605413..29606512 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 17q11.2-q21.1 XX CC Database Reference HGNC: 10618; CCL2 CC Database Reference ENTREZGENE: 6347 CC Database Reference UNIGENE: Hs.303649 CC Database Reference ENSEMBL: ENSG00000108691 CC Database Reference REFSEQ: NM_002982 CC Database Reference REFSEQ: NP_002973 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:216598_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:875_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:216598_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34375_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:216598_s_at CC Database Reference TRANSFAC GENE: G002972; MCP1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="17" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 29605413..29606512" FT /note="Genomic Strand: FORWARD" FT prim_transcript 999..>999 FT /db_xref="ENSEMBL:ENST00000225831" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: HSA [6356]; Alignment" FT /note="PRIMARY ANCHOR: HSA [6354]; Alignment" FT /note="PRIMARY ANCHOR: HSA [6356]; Alignment" FT /note="SECONDARY ANCHOR: HSA [6354]; Alignment" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:ADG04020" FT misc_feature 1002 FT /note="SECONDARY ANCHOR: RNO [24770]; Alignment" XX SQ Sequence 1100 BP; 261 A; 293 C; 241 G; 305 T; 0 other; gaacttcttg tccactgctg cctgctatgc tagcaacagc ctcctaactc ataatgactt 60 agccatgagg aatgtttcta gattctcctt tagctgtctg cccatttgga agatgctgag 120 gacagagaga ggacccaagc aggcaactag ttggaggact tgtacacgtt tccttccagc 180 agtatgtcag agaggtggca gcccactggg gacagggctg cctgggttct gtgctcgagg 240 ggaccttgag caggctattt aacccttctg tgcctcagtt gcctgatcta taacatgaaa 300 attagcaatc cctactagat aaagttgggg aatttacaga gttaatattt gtaaaggtct 360 gagaatattc ctggcagagt aagcactctg tgagtatgac actggcattt cttctgcagc 420 actacatgct gtctatgcct ttgtccaagt ctgaaaccct agaactctta gaattcagtt 480 caatgtttac acaatcctac agttctgcta ggcttctatg atgctactat tctgcatttg 540 aatgagcaaa tggatttaat gcattgtcag ggagccggcc aaagcttgag agctccttcc 600 tggctgggag gccccttgga atgtggcctg aaggtaagct ggcagcgagc ctgacatgct 660 ttcatctagt ttcctcgctt ccttcctttt ctgcagtttt cgcttcagag aaagcagaat 720 ccttaaaaat aaccctctta gttcacatct gtggtcagtc tgggcttaat ggcaccccat 780 cctccccatt tgctcatttg gtctcagcag tgaatggaaa aagtgtctcg tcctgacccc 840 ctgcttccct ttcctacttc ctggaaatcc acaggatgct gcatttgctc agcagattta 900 acagcccact tatcactcat ggaagatccc tcctcctgct tgactccgcc ctctctccct 960 ctgcccgctt tcaataagag gcagagacag cagccagagg aaccgagagg ctgagactaa 1020 cccagaaaca tccaattctc aaactgaagc tcgcactctc gcctccagca tgaaagtctc 1080 tgccgccctt ctgtgcctgc 1100 // ID HSA_6364_CCL20 standard; DNA; HUM; 1100 BP. XX AC 6364; XX DT 05-Sep-2005 (Created) XX DE CCL20: chemokine (C-C motif) ligand 20 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 228503069..228504168 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 2q33-q37 XX CC Database Reference HGNC: 10619; CCL20 CC Database Reference ENTREZGENE: 6364 CC Database Reference UNIGENE: Hs.75498 CC Database Reference ENSEMBL: ENSG00000115009 CC Database Reference REFSEQ: NP_004582 CC Database Reference REFSEQ: NM_004591 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205476_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205476_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40385_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205476_at CC Database Reference TRANSFAC GENE: G003484; SCYA20 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="2" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 228503069..228504168" FT /note="Genomic Strand: FORWARD" FT prim_transcript 995..>995 FT /db_xref="ENSEMBL:ENST00000233346" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [29538]; Alignment" FT prim_transcript 1007..>1007 FT /db_xref="ENSEMBL:ENST00000358813" FT misc_feature 1011 FT /note="SECONDARY ANCHOR: RNO [29538]; Alignment" XX SQ Sequence 1100 BP; 286 A; 230 C; 220 G; 364 T; 0 other; tttatttccg gtaacattaa aaaaaaatct attttgtctg atataggcat caccaactcc 60 agttctcttt tgtttactgt ttggtatacc tttcttttga tccttttact ttcaacctat 120 ttgggtctag tggagagttc ttatactgcc ttaggttagg gattcatatt acattatcat 180 cattagtact gttatttgac atttgctgtg ctgactagct actgctgata ggttttcttt 240 cctcaacaat tctgaggctc tatattgagt tatattagta catcatcatg gagagttaaa 300 ggtaggtaag gattattttc tgaactgcaa tattgattaa agccatgtga atgtataaga 360 ttcttagaag agttgacatt aaatcaaggt gaagctgagg tttgagcctt acttaaaggc 420 tgatattttc cactctaact gcggacagta ctgtagcact gttatagtac ctgctctgaa 480 tgttagtcta gcaactcagg gtcttcttca tgacagctga acctcaacca tgtgatggta 540 aatgtgtagc agagtatgcc tggcatccca cctgctcctc ctccccctcc tccttgactg 600 gttctggaaa gcaaataggg tgtaacaata ggagttctgg aatgttcctg tgtggggctg 660 acctttgtat cgctgttaat cctctatttt cagacacaaa aatgattaag ttaaaactgg 720 atgaaagtct tttctgggtc acagggctga gctgcttttg ctctttgcaa atacaaagaa 780 tttaacagga ttctcccctt ctcaacttcc tgtcccccac cctgaccttc gcaccttccc 840 aatatgagga aaaagcagga agttttcctt gcgggttttt tttatgatga catgatgggg 900 ccagttgatc aatggggaaa accccatgtg gcaacacgcc ttctgtgtac attcccaata 960 tttgctataa atagggccat cccaggctgc tgtcagaata taacagcact cccaaagaac 1020 tgggtactca acactgagca gatctgttct ttgagctaaa aaccatgtgc tgtaccaaga 1080 gtttgctcct ggctgctttg 1100 // ID HSA_6372_CXCL6 standard; DNA; HUM; 1100 BP. XX AC 6372; XX DT 05-Sep-2005 (Created) XX DE CXCL6: chemokine (C-X-C motif) ligand 6 (granulocyte chemotactic DE protein 2) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 75066427..75067526 (FORWARD) CC Score Points: 121 (98.4%) CC Chromosomal Location: 4q21 XX CC Database Reference HGNC: 10643; CXCL6 CC Database Reference ENTREZGENE: 6372 CC Database Reference UNIGENE: Hs.164021 CC Database Reference ENSEMBL: ENSG00000124875 CC Database Reference REFSEQ: NM_002993 CC Database Reference REFSEQ: NP_002984 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35410_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206336_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206336_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206336_at CC Database Reference TRANSFAC GENE: G003444; SCYB6 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 75066427..75067526" FT /note="Genomic Strand: FORWARD" FT prim_transcript 882..>882 FT /db_xref="dbTSS:CAS01639" FT prim_transcript 916..>916 FT /db_xref="dbTSS:CAS10890" FT prim_transcript 917..>917 FT /db_xref="dbTSS:SMR01349" FT prim_transcript 951..>951 FT /db_xref="dbTSS:SPL08305" FT prim_transcript 953..>953 FT /db_xref="dbTSS:CAS11037" FT prim_transcript 964..>964 FT /db_xref="dbTSS:CAS11356" FT prim_transcript 972..>972 FT /db_xref="dbTSS:SMR00991" FT prim_transcript 993..>993 FT /db_xref="dbTSS:SMR08742" FT /note="Number of reported TSSs: 2" FT misc_feature 996 FT /note="SECONDARY ANCHOR: HSA [6374]; Alignment" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:CAS08419" FT /note="Number of reported TSSs: 2" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:CAS00532" FT /note="Number of reported TSSs: 6" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [57349]; Alignment" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:SMR07650" FT /note="Number of reported TSSs: 7" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:CAS00194" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:CAS08283" FT /note="Number of reported TSSs: 20" FT prim_transcript 1005..>1005 FT /db_xref="EPD:EP73641" FT misc_feature 1005 FT /note="PRIMARY ANCHOR: MMU [57349]; Alignment" FT prim_transcript 1006..>1006 FT /db_xref="dbTSS:SMR05630" FT /note="Number of reported TSSs: 3" FT prim_transcript 1008..>1008 FT /db_xref="dbTSS:HRC03075" FT prim_transcript 1022..>1022 FT /db_xref="ENSEMBL:ENST00000226317" FT misc_feature 1077 FT /note="SECONDARY ANCHOR: MMU [57349]; Alignment" XX SQ Sequence 1100 BP; 234 A; 270 C; 244 G; 352 T; 0 other; tttttggttc catatgaact ttcaagtagt tttttccaat tctgtgaaga aagtcattgg 60 tagcttgatg gggatggtat tgaatctata agttaccttg ggcagtatgg ccatattcac 120 gatattgatt tttcctaccc atgagcatgg aatattcttc catttgtttg tatcctcttt 180 tatttcattg agcagtggtt tgtagttctc cttgaagagg tccttcatgt cccttgtaag 240 ttggattcct aggtatttta ttctctttga agcaattgtg aatgggagtt cactcatgat 300 ttggctctct gtttgtttgt tattggtgta taagaatgct tgtgattttt gtgcattgat 360 tttgtatcct gagactttgc tgaagttgct tatcagctta aggagatttt gggctgagac 420 catgtctctg tttgtttgtt attggtgtat aagaatgctt gtgatttttg tgcattgatt 480 ttgtatcctg agactttgct gaagttgctt atcagcttaa ggagattttg ggctgagacc 540 atggggtttt ctagatatac aattatgtaa tttgcaaata gggacaattt gacttcctct 600 tttcctaatt gaataccctt tatttccttc tcctgcctaa ttgtcctggc cattggagag 660 gaggagcatc tcccagacag ctgcgtgcct cagagaagcc agcctcgcta acccctcaag 720 cccaggggat gagaccctgc tgaatcgctg ctctattttg gctggagcca cagctccctc 780 caccgcgggg cggggctaaa atgtcctccc ccttaaggga gcaggcagct cctcccagcc 840 acccacccca ccaattccca tcctcccgcc cccctccacc aaccccttct ttccacactg 900 ccccctgagt tcagggaatt tccccagcat cccaaagctt gagtttcctg ccagtcggga 960 gggatgaatg cagataaagg gagtgcagaa ggcacgagga aaccaaagtg ctctgtatcc 1020 tccagtctcc gcgcctccac ccagctcagg aacccgcgaa ccctctcttg accactatga 1080 gcctcccgtc cagccgcgcg 1100 // ID HSA_6373_CXCL11 standard; DNA; HUM; 1100 BP. XX AC 6373; XX DT 06-Sep-2005 (Created) XX DE CXCL11: chemokine (C-X-C motif) ligand 11 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 77314342..77315441 (REVERSE) CC Score Points: 4 (66.7%) CC Chromosomal Location: 4q21.2 XX CC Database Reference HGNC: 10638; CXCL11 CC Database Reference ENTREZGENE: 6373 CC Database Reference UNIGENE: Hs.518814 CC Database Reference ENSEMBL: ENSG00000169248 CC Database Reference REFSEQ: NM_005409 CC Database Reference REFSEQ: NP_005400 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211122_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210163_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35061_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211122_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211122_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210163_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210163_at CC Database Reference TRANSFAC GENE: G003454; SCYB11 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 77314342..77315441" FT /note="Genomic Strand: REVERSE" FT prim_transcript 911..>911 FT /db_xref="ENSEMBL:ENST00000306621" FT prim_transcript 1011..>1011 FT /db_xref="dbTSS:LNF00940" FT prim_transcript 1037..>1037 FT /db_xref="dbTSS:LFL01886" FT prim_transcript 1040..>1040 FT /db_xref="dbTSS:LFL04636" XX SQ Sequence 1100 BP; 409 A; 208 C; 233 G; 250 T; 0 other; tataaagtag ctttccacca tggccaccat tggagggcag cagccatgac actgcactac 60 cctatagctg tgggcctcaa caagggccac aaggtgacca agaatgtgag caagcccagg 120 cacagccact gtgggcgcct gaccaaactc actaaatttg tgtgggacat gatcccagag 180 gtgtgtggct tcacccctaa cgagtggcgt ggcatggagt tactgaaggt ctccaaggtc 240 aaacaggccc tcaaattcat caagaaaagg gtagggacaa acatctgcac caagagaagg 300 caggaggagc tgagcaacgt cctggctgcc atgaggaaag cagctgccaa gaaggactga 360 gccccctgcc atctgcctat aatgaaagct ttgcagaata aaataaatat aaaataaagt 420 aataaaatta aattaaattt aaaaataaaa taaagcaaaa caaaataaaa tatataaagt 480 aaaaattgtt gaaaatgcaa aacaatatgg acataaatac agaaacacag ggaaacttct 540 ttaggcactc atttacaggt aaaaatatga aattgaataa aggtcatctg gtgtcaaata 600 atataggcct tatctattat aagagtttgg actgaaaagc aaaagtgaga taataaaaaa 660 aagcttttca gaatattatt ttgtatagat atgtgaagga tgaagggtgg gtgaaaggac 720 caaaaacaga aacacagtct tcctgaatga atgacaatca gaattccgct gcccaaagta 780 gtccgacaat taaatggatt tctaggaaaa gctaccttaa gaaggctggt taccatctgg 840 gttttcacag tgctttcaca ttcttatcac tttcaacact actgcaaata ggaagggaca 900 gtaacattta gaagagaaca aaacagaaac tcttggaagc aggaaaggtg catgactcaa 960 agagggaaat tcctgtgcca taaaaggatt gctggtgtat aaaatgctct atatatgcca 1020 attatcaatt tcctttcatg ttcagcattt ctactccttc caagaagagc agcaaagctg 1080 aagtagcagc agcagcacca 1100 // ID HSA_6374_CXCL5 standard; DNA; HUM; 1100 BP. XX AC 6374; XX DT 05-Sep-2005 (Created) XX DE CXCL5: chemokine (C-X-C motif) ligand 5 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 75229339..75230438 (REVERSE) CC Score Points: 8 (100.0%) CC Chromosomal Location: 4q12-q13 XX CC Database Reference HGNC: 10642; CXCL5 CC Database Reference ENTREZGENE: 6374 CC Database Reference UNIGENE: Hs.89714 CC Database Reference ENSEMBL: ENSG00000163735 CC Database Reference REFSEQ: NM_002994 CC Database Reference AFFYMETRIX: AFFY_HG_U95C:65970_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:214974_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:215101_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:214974_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35025_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:214974_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:215101_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:215101_s_at CC Database Reference TRANSFAC GENE: G004630; SCYB5 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 75229339..75230438" FT /note="Genomic Strand: REVERSE" FT prim_transcript 958..>958 FT /db_xref="dbTSS:KAT05668" FT prim_transcript 988..>988 FT /db_xref="ENSEMBL:ENST00000296027" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: HSA [6372]; Alignment" FT /note="PRIMARY ANCHOR: MMU [57349]; Alignment" FT prim_transcript 1010..>1010 FT /db_xref="dbTSS:SMR01342" FT /note="Number of reported TSSs: 5" FT prim_transcript 1012..>1012 FT /db_xref="dbTSS:SMR00905" XX SQ Sequence 1100 BP; 288 A; 311 C; 234 G; 267 T; 0 other; ctacaagaag ctttcacatg agcccttcaa actcatcagc ctcccacagc atctccaaat 60 ggtgtcaaat acatatctgg ggctgggaac agagctgggg caggcctggg atccctggca 120 agctttagcc tgcgctcacc atactacacc tcacccccaa caagaccaaa acctcttcca 180 attcaatagc atagcaactg ccaatagcaa ggtatcttcc atggcaattt gctgggtgat 240 tttggaagat ttttgtttaa ctacctggac acacgtatac ttgctatata ctacaagtac 300 agaattctca gtaagcggac ttaccaaagt aggtgatctg taggggagtt aacaaaattc 360 agtggtcctt tcaggccact gacttcaagt ggcaagagac aagggtctct tgttatcatg 420 ttatcttggc ttccaaagct ggttgaagtc cagagattca taaagtcatt caagaaacct 480 agaatgacct gcctgcaagg aagacaggaa ggactttcag tttatagcaa ttcaaacatg 540 aataacattt cctgattaat agtaataata attagaaagg attgactttc agaaattttt 600 ctcaaatcaa ggctcctgtt actttggttc caccttttct ctctagaagg agaggaggag 660 catctcccag agggctgcgt gcctcagaaa agccggcatc cctagcccgc tctggcacag 720 gccatgaggc cctgctgaat cctgctgaat agctactccc ttctagctgg agccacagct 780 ccctccaccg cggagcaggg ttacaacgtc cctctcggta gaggtgcacg cagctcctcc 840 tggccaccct ccccaccagt tcccattgtc tggcccccct cccccaacct cttctttcca 900 cactgcccca tgagttcagg gaatttcccc agcatcccaa agcttgagtt tcctgtcagt 960 ggggagagat gagtgtagat aaaaggagtg cagaaggcac gaggaagcca cagtgctccg 1020 gatcctccaa tcttcgctcc tccaatctcc gctcctccac ccagttcagg aacccgcgac 1080 cgctcgcagc gctctcttga 1100 // ID HSA_6376_CX3CL1 standard; DNA; HUM; 1100 BP. XX AC 6376; XX DT 06-Sep-2005 (Created) XX DE CX3CL1: chemokine (C-X3-C motif) ligand 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.16 55962893..55963992 (FORWARD) CC Score Points: 9 (81.8%) CC Chromosomal Location: 16q13 XX CC Database Reference HGNC: 10647; CX3CL1 CC Database Reference ENTREZGENE: 6376 CC Database Reference UNIGENE: Hs.531668 CC Database Reference ENSEMBL: ENSG00000006210 CC Database Reference REFSEQ: NM_002996 CC Database Reference REFSEQ: NP_002987 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:823_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:823_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203687_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:823_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:823_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203687_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203687_at CC Database Reference TRANSFAC GENE: G003458; SCYD1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="16" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 55962893..55963992" FT /note="Genomic Strand: FORWARD" FT misc_signal 731..771 FT /note="TRANSFAC Site R15809" FT prim_transcript 979..>979 FT /db_xref="dbTSS:HPR07257" FT prim_transcript 991..>991 FT /db_xref="dbTSS:AMR05841" FT /note="Number of reported TSSs: 2" FT prim_transcript 992..>992 FT /db_xref="dbTSS:AMR07012" FT /note="Number of reported TSSs: 2" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [20312]; Alignment" FT prim_transcript 1011..>1011 FT /db_xref="dbTSS:NRR06561" FT /note="Number of reported TSSs: 2" FT prim_transcript 1016..>1016 FT /db_xref="ENSEMBL:ENST00000006053" FT misc_feature 1018 FT /note="SECONDARY ANCHOR: MMU [20312]; Alignment" FT prim_transcript 1022..>1022 FT /db_xref="dbTSS:AMR07260" FT misc_feature 1074 FT /note="SECONDARY ANCHOR: RNO [89808]; Alignment" XX SQ Sequence 1100 BP; 211 A; 332 C; 338 G; 219 T; 0 other; aatgtgctcc caaggctggc aagcctctgc acccttcggt gagagcctgt tggagggccg 60 gtgctgggaa gccctctccc cattgcacta gcccaatgct ctctttgggc agatagagaa 120 ctcaggcccc acgagaggca agccttatcc aagccacggc tacagagttg aggagccaag 180 agccacagag ttatcgggga tgggttggca gccaccttgt tctttgggct aacaggggcc 240 agagcagagg tgggagtggg tgcaaagcag ggagcgggag accgggaggt ggaggcaggg 300 aggccagggc tctctcctgg gtcctgagct gtccacattc tgctcatcat ggtggtggga 360 ggggagttct ccactctgat gctgtggata acctggggtg gctccgggcc tcagtttccc 420 catctatcca tatgaagttg gactcaatcc ttctttcagc agaccctgca ccaagcccct 480 gctgacttca ggctccctgc tgggctctgg agatgcatag atcaacaagg tcccccagga 540 gcttgggatt ctaagagggg aaatttaggg gtccatcctg atgtgggcga ggcattctct 600 ggatcaaaga agagcttgtc agacccagga tggaggggcc ctgagtctct cccggcccct 660 tggcgccccg ctctctattc cacggcctgc tggccttttg tgtgttgccc acttaggatc 720 aagggcccca ggccagatcc tagggcatgt tcccagcttg tggcaggaga ggaggccttt 780 gtacccaggc aggcccagtc cagcctcccg gggaaggtcc cagtatgaca agcctaggat 840 ggtgagaagc ccagggacac aaagccggct tggttccttg gcaacatcct gaggaatcca 900 gcggctgcac actggctccc ttcctctccc ctcccaccct cctgcctgcg ggggctggag 960 gcggaggcag ccaaccccat tataaaaagc cacagatctc tggcggcggc aaggggacag 1020 cactgagctc tgccgcctgg ctctagccgc ctgcctggcc cccgccggga ctcttgccca 1080 ccctcagcca tggctccgat 1100 // ID HSA_6385_1_SDC4 standard; DNA; HUM; 1100 BP. XX AC 6385_1; XX DT 06-Sep-2005 (Created) XX DE SDC4: syndecan 4 (amphiglycan, ryudocan) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.20 43397797..43398896 (REVERSE) CC Score Points: 3 (10.7%) CC Chromosomal Location: 20q12 XX CC Database Reference HGNC: 10661; SDC4 CC Database Reference ENTREZGENE: 6385 CC Database Reference UNIGENE: Hs.252189 CC Database Reference ENSEMBL: ENSG00000124145 CC Database Reference REFSEQ: NM_002999 CC Database Reference REFSEQ: NP_002990 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35844_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202071_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202071_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202071_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="20" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 43397797..43398896" FT /note="Genomic Strand: REVERSE" FT prim_transcript 933..>933 FT /db_xref="dbTSS:SMR08917" FT prim_transcript 1034..>1034 FT /db_xref="dbTSS:JTH07382" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 235 A; 290 C; 299 G; 276 T; 0 other; ggtctgggca gcgccctgac ctgaggctgt cttagggtgt gcgtgaggca gccctgtctg 60 tcccggccca gactgactca gctgggaaaa gtatcctgga ctgggcaaga ccagaaccag 120 gagcccactc cctgtcctgt gtgaatcagc tgccactgca tcacagagcc ctggagtgta 180 gcatcccagg gccctgtgca tggagactcc tggctctgaa gtcaggcagc cctgcgtatg 240 caatcctcgc tcttccatct gccagctgtg tcaccaaaag aaaatgactc cctcggctgt 300 aaaaagaagt gaataacatg cctccagagt tattaaaaca gggcccagca catagcaagt 360 gctcggtaaa ggatatctag ccatattaat aatttgatta ttacctcatt tactgttttt 420 attttttttg agacgggggt cccactctgt agctcaggct agagtgcaac ggcgtgatcc 480 tggcttattg caacctccgc ctcccgggtt caagcaattc tcctgtctca gcctcccgag 540 tagctgggac tacaggcgta agccaccacg cccagctgat ttttgtattt ttagtagaga 600 cggggtttca ccatgttggc caggctggtc ttgaactcct gacctcaagt gatctgcctg 660 cctccgcctc ccaaagtgtt gggattacag gtgtgagcca ctgtgcccag cctcatgtac 720 tatttttatt tgcccagaat ggaaagagac ttgcctaagg acacgcggtg agttagaggt 780 agagtgggat ccaggacgca ggtctccagg ccctggcctg gtctctttct agtttctgaa 840 tgcccacttc actagctttt gggcatcagc tgtcatggag cactggggat gttggctgat 900 gtgtctcctt tctttatctt agatccgaga gactgaggtc atcgaccccc aggacctcct 960 agaaggccga tacttctccg gagccctacc agacgatgag gatgtagtgg ggcccgggca 1020 ggaatctgat gactttgagc tgtctggctc tggagatctg ggtacggaag gtgtgctggg 1080 caggcgtagg cacaaagctg 1100 // ID HSA_6401_SELE standard; DNA; HUM; 1100 BP. XX AC 6401; XX DT 06-Sep-2005 (Created) XX DE SELE: selectin E (endothelial adhesion molecule 1) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 166434738..166435837 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 1q22-q25 XX CC Database Reference HGNC: 10718; SELE CC Database Reference ENTREZGENE: 6401 CC Database Reference UNIGENE: Hs.89546 CC Database Reference ENSEMBL: ENSG00000007908 CC Database Reference REFSEQ: NM_000450 CC Database Reference REFSEQ: NP_000441 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206211_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:265_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206211_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206211_at CC Database Reference TRANSFAC GENE: G000248; SELE XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 166434738..166435837" FT /note="Genomic Strand: REVERSE" FT misc_signal 794..831 FT /note="TRANSFAC Site R11552" FT misc_signal 863..877 FT /note="TRANSFAC Site R03275" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000333360" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [20339]; Alignment" FT /note="PRIMARY ANCHOR: RNO [25544]; Alignment" XX SQ Sequence 1100 BP; 308 A; 227 C; 222 G; 343 T; 0 other; agagtttcac tcgtttccca ggctggagtg cactggcgtg atcttggctc actgcaacct 60 ccacttcccg ggttcaagcg attctcctgc ctcagcctcc cgagtagctg ggattacagg 120 catgcgccac catgcccagc taattttgta tttttagtag agatggcgtt tctccatgtt 180 ggtcaggctg gtcttgaact cccggcctca ggtgatccgc ctgcctcggc ctcccaaagt 240 ggtgggatta caggcgtgag ccactgtgcc tggcctcctt tttatttttt tcactgaaca 300 aaccatgaaa ctttcccaga tgtaaatatc tatttcccat ttttcttttt ttaaaataag 360 gcattatttt aaccatttga gtgttagata ttatttttag ataatatttt aatttaggca 420 taactgccgt gcaaaatctg aagattaata tctaccttgt gagtcattcc tctgtgagac 480 agtgcatgtt aaatatgttg aattggcagg tgaaaaagga agaaaaaatg agtagtgatt 540 ggttatccac agctatgaat gagaaattga aggtagtaga ctatggatga caaacctatt 600 cttggtttcc ttctgtttct gaaattctaa ttactaccac aactacatga gagacactac 660 taacaagcaa agttttacaa ctttttaaag acatagactt tatgttatta taattaaaaa 720 tcatgcattt ttgtcatatt aataaaattg catatacgat ataaaggcat ggacaaaggt 780 gaagtagctt caagagacag agtttctgac atcattgtaa ttttaagcat cgtggatatt 840 cccgggaaag tttttggatg ccattgggga tttcctcttt actggatgtg gacaatatcc 900 tcctattatt cacaggaagc aatccctcct ataaaagggc ctcagccgaa gtagtgttca 960 gctgttcttg gctgacttca catcaaaact cctatactga cctgagacag aggcagcagt 1020 gatacccacc tgagagatcc tgtgtttgaa caactgcttc ccaaaacggt aagtgcagaa 1080 cgctttataa gggcagcctc 1100 // ID HSA_64135_IFIH1 standard; DNA; HUM; 1100 BP. XX AC 64135; XX DT 07-Sep-2005 (Created) XX DE IFIH1: interferon induced with helicase C domain 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 163000521..163001620 (REVERSE) CC Score Points: 5 (62.5%) CC Chromosomal Location: 2p24.3-q24.3 XX CC Database Reference HGNC: 18873; IFIH1 CC Database Reference ENTREZGENE: 64135 CC Database Reference UNIGENE: Hs.163173 CC Database Reference ENSEMBL: ENSG00000115267 CC Database Reference REFSEQ: NM_022168 CC Database Reference REFSEQ: NP_071451 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219209_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219209_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:51920_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219209_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="2" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 163000521..163001620" FT /note="Genomic Strand: REVERSE" FT prim_transcript 900..>900 FT /db_xref="dbTSS:LFL09517" FT prim_transcript 911..>911 FT /db_xref="dbTSS:LFL07731" FT prim_transcript 952..>952 FT /db_xref="dbTSS:LFL01295" FT prim_transcript 1075..>1075 FT /db_xref="ENSEMBL:ENST00000263642" XX SQ Sequence 1100 BP; 271 A; 301 C; 238 G; 290 T; 0 other; ttttttctct catgacatag acaaatgttg atgtttacta caagttggta cattagttgc 60 taattaagtt cctagctgct ccagccaaaa cttgctgtat tgaatccaag aaaagaatgg 120 cagctatatc aaaaataagt tgttggggga tttttttgtt ttgttttatt aaaggaaagt 180 tgtatattaa agaatatagg gaacttacaa gctgggatct aggaaacttt aagtcttggc 240 ttccttctaa gctgagttgg tggttcaagt ccatccacat ctgttaccag gtcctggtca 300 aagctgcata aataccagca atctaaatat gaggcagtaa agttaactgt ttattgttac 360 tcactttttc gaacccacct ccaaattccc agggaaacaa gttagtgttt gggaacccac 420 aggaggtcag gtttatttta ggaaggactt cctcctgtct tctccacatc tctgcaaaga 480 tgtcttctga gcttcatctc tcacctgtcc ctcgcagtct caccaccctc agccaggcct 540 gcctacattc accagccgag ggtaactccc tgttcacgtc cgggtctgtg gcagtttctg 600 ttcacttccc ctttggaaag tcccaaatca catgctttta tgccctgcac attttggcct 660 acaaaggacc ttattgttaa ggcagaacct gctgggaaaa caaaatatcc gccggaggag 720 ctttgctaga gcgttggtct tggtgtcaga gagaattcgc tttccttttc tgtttcccgc 780 ggtgtcctta accaaaggcc tcctctcttc acccgccccg accaaaaggt ggcgtctccc 840 tgaggaaact ccctccccgc caggcagatt acgtttacaa agtcctgaga agagaatcga 900 aacagaaacc aaagtcaggc aaactctgta agaactgcct gacagaaagc tggactcaaa 960 gctcctaccc gagtgtgcag caggatcgcc ccggtccggg accccaggcg cacaccgcag 1020 agtccaaagt gccgcgcctg ccggccgcac ctgcctgccg cggccccgcg cgccgccccg 1080 ctgcccacct gcccgcctgc 1100 // ID HSA_650_BMP2 standard; DNA; HUM; 1100 BP. XX AC 650; XX DT 06-Sep-2005 (Created) XX DE BMP2: bone morphogenetic protein 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.20 6695745..6696844 (FORWARD) CC Score Points: 1 (50.0%) CC Chromosomal Location: 20p12 XX CC Database Reference HGNC: 1069; BMP2 CC Database Reference ENTREZGENE: 650 CC Database Reference UNIGENE: Hs.73853 CC Database Reference ENSEMBL: ENSG00000125845 CC Database Reference REFSEQ: NP_001191 CC Database Reference REFSEQ: NM_001200 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205290_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40367_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205289_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205290_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205289_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205290_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:59306_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1113_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205289_at CC Database Reference TRANSFAC GENE: G003352; BMP2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="20" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 6695745..6696844" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000246044" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [12156]; Alignment" FT /note="PRIMARY ANCHOR: RNO [29373]; Alignment" XX SQ Sequence 1100 BP; 191 A; 388 C; 342 G; 179 T; 0 other; acacatttat gtaaaaaaat ttgtacacat gcatttacat atgtaaatac atacatctct 60 atgtattaat gtttaaaaac actcaatttc cagcctgctg ttttctttta attttcctcc 120 tattccgggg aaacagaagc gtggatccca cgtctatgct atgccaaaat acgctgtaat 180 tgaggtgttt tgttttgttt tgttttttga aatcgtatat taccgaaaaa cttcaaactg 240 aaagttgaat aacgggccca gcggggaaat aagaggccag accctgaccc tgcatttgtc 300 ctggatttcg cctccagagt ccccgcgagg gtccggcgcg ccagctgatc tctcctttga 360 gagcagggag tggaggcgcg agcgcccccc ttggcggccg cgcgcccccg ccctccgccc 420 caccccgccg cggctgcccg ggcgcgccgt ccacacccct gcgcgcagct cccgcccgct 480 cggggatccc cggcgagccg cgccgcgaag ggggaggtgt tcggccgcgg ccgggaggga 540 gccggcaggc ggcgtcccct ttaaaagccg cgagcgccgc gccacggcgc cgccgccgcc 600 gtcgccgccg ccggagtcct cgccccgccg cgctgcgccc ggctcgcgct gcgctagtcg 660 ctccgcttcc cacaccccgc cggggactgg cagccgccgc cgcacatctg ccgccacagc 720 ctccgccggc tacccgaacg ttctcggggc cagcgccgag tggatcaccg gggaccgcga 780 ggcacccgcg cgccgcagac cccgcgcggg ctggagcacc cggcagagcg cgccacagcg 840 ccgtggcctc tgctgcccgg gctgcgccag agccgcggac gggcgcgcag agcgccgggg 900 actccggagc cgatccctag cgccgcgatg cggagcacct actgcaggag atcgggggcc 960 tgggacgcgc tggccgaggt gtgatcggac cccaggctag ccacaaaggg cacttggccc 1020 cagggctagg agagcgaggg gagagcacag ccacccgcct cggcggcccg ggactcggct 1080 cgactcgccg gagaatgcgc 1100 // ID HSA_6542_SLC7A2 standard; DNA; HUM; 1100 BP. XX AC 6542; XX DT 06-Sep-2005 (Created) XX DE SLC7A2: solute carrier family 7 (cationic amino acid transporter, y+ DE system), member 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 17397976..17399075 (FORWARD) CC Score Points: 1 (33.3%) CC Chromosomal Location: 8p22-p21.3 XX CC Database Reference HGNC: 11060; SLC7A2 CC Database Reference ENTREZGENE: 6542 CC Database Reference UNIGENE: Hs.448520 CC Database Reference ENSEMBL: ENSG00000003989 CC Database Reference REFSEQ: NM_003046 CC Database Reference REFSEQ: NM_001008539 CC Database Reference REFSEQ: NP_001008539 CC Database Reference REFSEQ: NP_003037 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38169_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207626_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207626_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40236_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207626_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 17397976..17399075" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:Zrv6c570.seq" XX SQ Sequence 1100 BP; 244 A; 337 C; 279 G; 240 T; 0 other; ttactccaat actatgcaaa gtaaagtgga cctttctgtc aaacaaaaat agtaataggc 60 cgggcatggt ggctcaagcc tgtaattctc agcctggtgg ctcaagcctg taattgtcag 120 cactttggga ggctgaggcg ggaggatagc ttgagcccag gaggtcgagg ctgcagtgag 180 ccacgattgt gtcactgccc tccagcctgg gcgacagagt gagaccctgt ctctaaagac 240 aaaccacaca cacatataca cacacacact gacacacact tattgttcaa ttcagtgcgt 300 gttttgcttc gttttggatg aaaattaaca ggctttcaca ttgtgactta atcttatcag 360 agactcctaa agtaaacaat agcgcagtag gagaaaccct gattgtgtaa cttctgctct 420 tgctcccctg gaaataatgt catttcctat aaacccaccc ccaaacaatc gtgactacgt 480 attcatacca ctggagtctt ccaaaatagc aactgcacat tatttatcaa cgtttagttt 540 gcatttgaca aagcacatcc acctgggctt ccatttatca ttgctattat tatattttat 600 tattattttc ttatttccaa aatctttcta gaatggaaag taaacggggg gaccaaaacc 660 ccacttagaa ctctgcttag aagattcgga aatgcccttg aggtttggtc ctcccaggag 720 agcacgaagt ttatcctcgc gcgcagcctc tcttccccgg cccgcgccca ccggcctagc 780 ccggggctag cgcccgccca cgtgtgctcg gctccaggca aaccccgctg agcagcggcc 840 gcacaccgcc caccccgggg attggccagc gcggccgggg cccggcggga ggcgggctcg 900 gggtcgcgtt ccgggagcgc ggaggaggcg gtgccgcccg gccccgcgcc ccgcccccgc 960 cccgggtggc tacacagagg ggcgcccacg tgcccagccc tccttctgca gcgcggccgg 1020 cgggcgctcc tcttcccggg accagcgagg cggcggccgc tgctccagcg tcccccagcc 1080 gcgggccccc gacgcgctgc 1100 // ID HSA_6558_SLC12A2 standard; DNA; HUM; 1100 BP. XX AC 6558; XX DT 06-Sep-2005 (Created) XX DE SLC12A2: solute carrier family 12 (sodium/potassium/chloride DE transporters), member 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 127446374..127447473 (FORWARD) CC Score Points: 3 (37.5%) CC Chromosomal Location: 5q23.3 XX CC Database Reference HGNC: 10911; SLC12A2 CC Database Reference ENTREZGENE: 6558 CC Database Reference UNIGENE: Hs.162585 CC Database Reference ENSEMBL: ENSG00000064651 CC Database Reference REFSEQ: NM_001046 CC Database Reference REFSEQ: NP_001037 CC Database Reference AFFYMETRIX: AFFY_HG_U133B:225835_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:225835_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:65492_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204404_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204404_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37423_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:58621_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204404_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 127446374..127447473" FT /note="Genomic Strand: FORWARD" FT prim_transcript 984..>984 FT /db_xref="ENSEMBL:ENST00000343225" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [20496]; Alignment" FT prim_transcript 1009..>1009 FT /db_xref="ENSEMBL:ENST00000262461" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 166 A; 374 C; 414 G; 146 T; 0 other; cacccactgc atcacaactg gaactgatct ctggttatgc caatctaggt ctgcctggca 60 gggtgagtct accgctcgaa agctgcacag aggaaatcct ccctcctcca ggttcaggcc 120 cggagttacg agcggagatt cgcggcggcg ggtcagagcc cagagcaaac caggctgggg 180 aacgcacctc gcccgcggct ccggaagcgg ctgcggcccc gaccggaaag cccccagcat 240 cgcccgaagg aatcgcggct ggcctgcggc tccggcccgg cctcgggtac cacgcgccta 300 gtgggaagcc gcactgacgc ctgcagcatc tcgcgagatt tcgggctcag cccaagtact 360 gcgagttcac caaagcgggg ggaaaaaaaa aaagccagcg tgcgagagcc tctgaagccg 420 tggctggggc gctggggtgg cagctgccgc gggagcatca gctaccggcg tgaggcgagg 480 cagggcacgc gcgccgtccg cagccccgtt gcctgggctg caggtccact gacgcgcggc 540 ccctgggtgg agagagggga ggtggcctgg gagcccgctc cttttcgccg cagagcgcgg 600 cgggggaggg aggtgaaggc gtgggaggaa ggcggcggaa gaggaggtag ccgcgcggag 660 atcctcccgg cgacatcact gaggcggagc gtagccgcgc ctgctccccg atcgcgccgt 720 tcgtgctgcc cgcactgccc gaggcccttt gcggactggc tggccgcgct cttcgcacgg 780 ggcgcttttg cgtggggtcg cgcaggagcc gcggagggcc ggatcgctga gggagcgtca 840 gccgcgcgcc gctgcgggac cgcgggtggg cgggctgagg ggcggaggag cctccggccc 900 cgcctcccgc gtgctgctgc cggagccgcc gccgccgcag ccccgccgag gctttaaaca 960 gcggggcccg ccccgcgccc gccacactcg cgcgctcgct cggctgccgg tggcctctgt 1020 ggccgtccag gctagcggcg gcccgcaggc ggcggggaga aagactctct cacctggtct 1080 tgcggctgtg gccaccgccg 1100 // ID HSA_6648_SOD2 standard; DNA; HUM; 1100 BP. XX AC 6648; XX DT 05-Sep-2005 (Created) XX DE SOD2: superoxide dismutase 2, mitochondrial XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 160084587..160085686 (REVERSE) CC Score Points: 76 (96.2%) CC Chromosomal Location: 6q25.3 XX CC Database Reference HGNC: 11180; SOD2 CC Database Reference ENTREZGENE: 6648 CC Database Reference UNIGENE: Hs.487046 CC Database Reference ENSEMBL: ENSG00000112096 CC Database Reference REFSEQ: NM_000636 CC Database Reference REFSEQ: NM_001024465 CC Database Reference REFSEQ: NP_001019636 CC Database Reference REFSEQ: NP_000627 CC Database Reference REFSEQ: NP_001019637 CC Database Reference REFSEQ: NM_001024466 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:216841_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:216841_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:215223_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:215223_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:215223_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:73312_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:216841_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34666_at CC Database Reference TRANSFAC GENE: G018710; SOD2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 160084587..160085686" FT /note="Genomic Strand: REVERSE" FT prim_transcript 934..>934 FT /db_xref="dbTSS:MPC06855" FT prim_transcript 962..>962 FT /db_xref="dbTSS:SMR01128" FT prim_transcript 966..>966 FT /db_xref="dbTSS:NRR06953" FT /note="Number of reported TSSs: 2" FT prim_transcript 970..>970 FT /db_xref="dbTSS:CAS08871" FT prim_transcript 973..>973 FT /db_xref="dbTSS:HKR03303" FT /note="Number of reported TSSs: 2" FT prim_transcript 999..>999 FT /db_xref="dbTSS:MPE04971" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:HKR11549" FT /note="Number of reported TSSs: 3" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:SMR04459" FT /note="Number of reported TSSs: 4" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:HKR04550" FT /note="Number of reported TSSs: 2" FT prim_transcript 1003..>1003 FT /db_xref="EPD:EP73767" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:STM06834" FT prim_transcript 1020..>1020 FT /db_xref="ENSEMBL:ENST00000358304" FT prim_transcript 1051..>1051 FT /db_xref="dbTSS:w0713.seq" FT prim_transcript 1073..>1073 FT /db_xref="ENSEMBL:ENST00000337404" XX SQ Sequence 1100 BP; 214 A; 316 C; 378 G; 192 T; 0 other; aactgttgag agagcacttg atacttaaca gcttactagg ctacaagaca gcgcaggaaa 60 gaatcctctg ttgtcctttt atgttatcct gaacagttgg ttcacagagt tactgtaaac 120 acacaaaaca tgactgccag ggcttagtag tgaggaaggt gggaactagt cctgactcag 180 ttaactgtgc ccaggagaag ctgcttaacc tcaaaggatt tcactattac tagaatcaat 240 aataccaacc ctaggggtaa aaataaagat aaatgtgtgc aaatcctgcc tgcagtctcg 300 ggcacgtcgt gggtgtccaa gaactgttct taggcagccg gtggggacaa agtctgtgtg 360 cctcctgtcc tggaataggt cccaaggtcg gcttacttgc aaagcaaggg tacggcgcaa 420 gagtactgaa tacgggttgg aagggcgctg gctctaccct cagctcatag gccggctggg 480 cggcgctgac cagcagctag gccccgtctt ccctaggaac ggccacgggg gccctgggag 540 ggtatgaatg tctttttgca gtgaggcctc tggaccccgc ggccccccgg cagcgcaacc 600 aaaactcagg ggcaggcgcc gcagccgcct agtgcagcca gatccccgcc ggcaccctca 660 ggggcggagc cggaggcagg gccttcgggc cgtaccaact ccacgggggc aggggccgcc 720 tcccttcggc cgcgcgccac tcaagtacgg cagacaggca gcgaggttgc cgaggccgag 780 gctagcctgc agcctccttt ctcccgtgcc ctgggcgcgg ggtgtacggc aagcgcgggc 840 gggcgggaca ggcacgcagg gcacccccgg ggttgggcgc ggcgggcgcg gggcggggcc 900 cgcggggggg gggggcgggg cggcggtgcc cttgcggcgc agctggggtc gcggccctgc 960 tccccgcgct ttcttaaggc ccgcgggcgg cgcaggagcg gcactcgtgg ctgtggtggc 1020 ttcggcagcg gcttcagcag atcggcggca tcagcggtag caccagcact agcagcatgt 1080 tgagccgggc agtgtgcggg 1100 // ID HSA_6890_1_TAP1 standard; DNA; HUM; 1100 BP. XX AC 6890_1; XX DT 06-Sep-2005 (Created) XX DE TAP1: transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 32924607..32925706 (REVERSE) CC Score Points: 2 (5.6%) CC Chromosomal Location: 6p21.3 XX CC Database Reference HGNC: 43; TAP1 CC Database Reference ENTREZGENE: 6890 CC Database Reference UNIGENE: Hs.352018 CC Database Reference ENSEMBL: ENSG00000168394 CC Database Reference REFSEQ: NM_000593 CC Database Reference REFSEQ: NP_000584 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40153_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202307_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202307_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202307_s_at CC Database Reference TRANSFAC GENE: G014205; Tap1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 32924607..32925706" FT /note="Genomic Strand: REVERSE" FT prim_transcript 839..>839 FT /db_xref="dbTSS:MPG02817" XX SQ Sequence 1100 BP; 219 A; 266 C; 254 G; 361 T; 0 other; gaatagtgga agccagggat gagggacatc tgtgatgcac tggaaagaga gctacgccag 60 tgatccgaag atcctggctt gatgatgcaa tttacttgtc ttgtgatcat gacaacaaat 120 ttaccttctc tgagactgtt tcctctttat ttatttattt gtttgtttgt ttgtttattt 180 ttacttatta ttattatttt tgagctggag tctcgctttg tcgcccaggc tggagtgcag 240 tggcgcgatc tgggctcact gcaagctccg cctcccgggt tcacgccgtt ctcccgcctc 300 agcctcctga gtagctggga ctacaggcac ccgccaccac gcccggctaa tttttttttt 360 ttttttgtat ttttagtaga gacgaggttt ctccgtgtta gccaggatgg tctcaatctc 420 ctgaccttgt gatccgccca cttcggcctc ccaaagtgct ggaattgcag gcatgagcca 480 ctgcgcccga ctggttgttt cctcattttt caaaaatgga gtgatataac cttctttata 540 aggctcttca tgtattagct gacatcacat gaatgaaagc cttttgtgaa gagtaaaatg 600 ctccccagac aaggtgatag tggtgatggt ggtgaagata actgtgactt gcatgatgtg 660 cattgagtca gactccatgg ggtctctggt tcattctcct gtctgcctat tgagcctgcc 720 gatgtcactt aggagacagg gacttgatat ttccttcagg ttaatgactg cggttctttg 780 tgtcccctcc agatttctct acctcagtcc ctttttttgt ggtctcttta tagatttcag 840 gtatgctgct gaaagtggga atcctctaca ttggtgggca gctggtgacc agtggggctg 900 taagcagtgg gaaccttgtc acatttgttc tctaccagat gcagttcacc caggctgtgg 960 aggtgaggtc cctccacctt cactccccag tgtgattcct tcctctggcc cagcaccatc 1020 tgtgtgatgt ccttccattc tttacccttc ttgcttcaca taatgctggc aagcagacta 1080 cctcactttc actattctta 1100 // ID HSA_6890_4_TAP1 standard; DNA; HUM; 1100 BP. XX AC 6890_4; XX DT 06-Sep-2005 (Created) XX DE TAP1: transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 32927853..32928952 (REVERSE) CC Score Points: 2 (5.6%) CC Chromosomal Location: 6p21.3 XX CC Database Reference HGNC: 43; TAP1 CC Database Reference ENTREZGENE: 6890 CC Database Reference UNIGENE: Hs.352018 CC Database Reference ENSEMBL: ENSG00000168394 CC Database Reference REFSEQ: NM_000593 CC Database Reference REFSEQ: NP_000584 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40153_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202307_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202307_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202307_s_at CC Database Reference TRANSFAC GENE: G014205; Tap1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 32927853..32928952" FT /note="Genomic Strand: REVERSE" FT prim_transcript 994..>994 FT /db_xref="dbTSS:COL08109" FT prim_transcript 1009..>1009 FT /db_xref="dbTSS:T3R09371" XX SQ Sequence 1100 BP; 222 A; 274 C; 339 G; 265 T; 0 other; cactgcccgc agcagccctg tggcacaaac tcgggagcct ctgggtgccc ggcggtcagg 60 gcggctctgg aaaccctgtg cgtcggcttc taggctgcct gggctcggag acgcgccgcc 120 tctcgctgtt cctggtcctg gtggtcctct cctctcttgg taaggggaac gcagggcaag 180 aggggaggac acaaggggac tgggacagga atcaaaggta attgtcagta aggtagagta 240 gcgtgggttc tgggaaatgt ggagcaggag aaggactcct agcgtgggtc ttggaacacc 300 acttcggtgt agaagaaacg gcactggact ggcgggggcc agaggttctg ggctccattg 360 ctgaccgggt cttgattctt tgggccacgc cggaagcggg gaaatccttt gctctggggc 420 cgaagggcgg ggcatcctca tctctaacag gaggcttttc tacttcatga tctccagcct 480 tcctaataaa atcctgaaag ttctggtaga gcaaccacag ggtagtgagt tccagggcag 540 cctatttagg ttcgggattg agacgtcagt gtttcctttc tgctgatgcc ctccaggata 600 atggtgaggg ggaggaggcg tggtggggcc agtctgactg gaactgacct acttagactt 660 aatatttgtg cgtgacctct cttctctttc tccaggggag atggccattc cattctttac 720 gggccgcctc actgactgga ttctacaaga tggctcagcc gataccttca ctcgaaactt 780 aactctcatg tccattctca ccatagccag gtctgggggc tgaaaatggg gcaccctgca 840 aatgagggag ttggaagttg gggctgctgt ccgaaatgca cttatatggg gatacctggg 900 accttcagtc tgttccctga acacaccctg atcccctttt tttccgggtt ctttatagtg 960 cagtgctgga gttcgtgggt gacgggatct ataacaacac catgggccac gtgcacagcc 1020 acttgcaggg agaggtgttt ggggctgtcc tgcgccagga gacggagttt ttccaacaga 1080 accagacagg tttctcctga 1100 // ID HSA_7126_1_TNFAIP1 standard; DNA; HUM; 1100 BP. XX AC 7126_1; XX DT 06-Sep-2005 (Created) XX DE TNFAIP1: tumor necrosis factor, alpha-induced protein 1 (endothelial) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.17 23685933..23687032 (FORWARD) CC Score Points: 78 (88.6%) CC Chromosomal Location: 17q22-q23 XX CC Database Reference HGNC: 11894; TNFAIP1 CC Database Reference ENTREZGENE: 7126 CC Database Reference UNIGENE: Hs.76090 CC Database Reference ENSEMBL: ENSG00000109079 CC Database Reference REFSEQ: NP_066960 CC Database Reference REFSEQ: NM_021137 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201208_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201207_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36988_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201208_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201208_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201207_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201207_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="17" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 23685933..23687032" FT /note="Genomic Strand: FORWARD" FT misc_feature <1..818 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT misc_feature 184..1000 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT prim_transcript 794..>794 FT /db_xref="dbTSS:TDR00348" FT prim_transcript 925..>925 FT /db_xref="dbTSS:UBA07340" FT prim_transcript 945..>945 FT /db_xref="dbTSS:WMC05176" FT prim_transcript 960..>960 FT /db_xref="dbTSS:LFL08621" FT prim_transcript 981..>981 FT /db_xref="ENSEMBL:ENST00000226225" FT prim_transcript 982..>982 FT /db_xref="dbTSS:TIR03833" FT /note="Number of reported TSSs: 4" FT prim_transcript 984..>984 FT /db_xref="dbTSS:TDR03253" FT /note="Number of reported TSSs: 9" FT prim_transcript 987..>987 FT /db_xref="dbTSS:LNG11142" FT prim_transcript 988..>988 FT /db_xref="dbTSS:KAT02360" FT prim_transcript 992..>992 FT /db_xref="dbTSS:TDR00692" FT prim_transcript 998..>998 FT /db_xref="dbTSS:SZB01369" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:UBA03515" FT prim_transcript 1010..>1010 FT /db_xref="EPD:EP74484" FT prim_transcript 1015..>1015 FT /db_xref="dbTSS:OFR01244" FT prim_transcript 1033..>1033 FT /db_xref="dbTSS:Hc-0034.seq" FT prim_transcript 1034..>1034 FT /db_xref="dbTSS:LFL04918" FT /note="Number of reported TSSs: 2" FT prim_transcript 1045..>1045 FT /db_xref="dbTSS:CNR03809" XX SQ Sequence 1100 BP; 224 A; 347 C; 339 G; 190 T; 0 other; gtaagtcgag gtgatggggc ttagcaatgg actgactgaa tgtgggggtt tggggataag 60 agaaaaacaa gtcaggcatg actcccatga atctggcttg gcccacctat ctgattggaa 120 gggctggctt aaagagatag gtaagatgga agaagaggtg cagggaaaga gttcacagat 180 tatctaccaa ctcccatcac acgcgtgtct gagcatctga gcaacacctg gcccaagagc 240 tgggactaag ctccctgagc atgaggcggt ggcatacttt ctgcgccccg gctctcccag 300 atgcatgcga ggcactgcga gccgactctt tactatgtaa actccccgaa cttatccgag 360 ccgcagtttc ctcgtaagat cgtggcaagc atcaacgcat caaactccag gcctaagctg 420 ggtgtgaaag cgcccccctg agagtggggc ggaattccca cgtctctccc cgcccggtac 480 tgcctttcct caggacgcgg gcctgtcagg ctcctctcgc ccctggtccg cccgcgtccc 540 ccgacccgag gtcagcctac ctgccggccc cgcggcggca gcgcgctgca gcccaggctg 600 atgtagacag gcagcttctc ctgggtcagc gacagccggt acccagccag cctgccacgg 660 ccgctgccac ggatacagag cctgtttacc tatgacgtca ctaccttcct gactccggaa 720 gcacttacag cccccattcc acagagcctg ctgggaaaca gaggcccgag gggaggcccg 780 gcctacaaga cccagaagcc ttagcgccgg caaggcggcc agaagtagct ctgctctctc 840 cgcgaagacc ctcgggggat tccgcctcca ccctttcccg gatagagcgc tatgcatgca 900 gggacttgta gtctcaggct ccccagccgg ctgggctggg cagcactccg ggcggagtcg 960 acgagcgcag gatgtgagct cacagcttgg gactgctgag gggcaggcgg ctgcaggcta 1020 ggggcggctc ggagtccgct ggccacccag ctgagaggag aggcgccccc ggggacggtg 1080 agagccgggc ccgccgatgc 1100 // ID HSA_7127_TNFAIP2 standard; DNA; HUM; 1100 BP. XX AC 7127; XX DT 06-Sep-2005 (Created) XX DE TNFAIP2: tumor necrosis factor, alpha-induced protein 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.14 102658551..102659650 (FORWARD) CC Score Points: 1 (14.3%) CC Chromosomal Location: 14q32 XX CC Database Reference HGNC: 11895; TNFAIP2 CC Database Reference ENTREZGENE: 7127 CC Database Reference UNIGENE: Hs.525607 CC Database Reference ENSEMBL: ENSG00000185215 CC Database Reference REFSEQ: NM_006291 CC Database Reference REFSEQ: NP_006282 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202509_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202509_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202510_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38631_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202509_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202510_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202510_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:74633_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="14" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 102658551..102659650" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:THR08301" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [21928]; Alignment" XX SQ Sequence 1100 BP; 180 A; 392 C; 353 G; 175 T; 0 other; attcctaaat gtctgggtcc tttccagagg gcaggaattc ctagcctaga gtgtgaaata 60 aggaaggaag tgaatctcca gtgggttccc ttcacagccc ctttccatcc tccccacatg 120 ccccaccccc acatctccca aaacaaaccc tgagagacgg tgtggatggg gagacaggcc 180 tggaaacgga ggcctgcgct gaatgggcaa agccgggttg atgatccaga cgaggccctg 240 gagtctgggc cttgggcccc tccccttctg cctgctccgg cagcctgtgg gtccagcccc 300 agccccagag ggggaaaggc tccagtggga gtcccatagg cctggctagg aaccccactc 360 cgctacttaa agtggtgtga gccgggtcag ccacttcacc tttccgcatt tacgcatttc 420 aagcaaggct tgacgaccgg aggggctcaa ggccctgtgc acagccgcgc ggccagcact 480 ctggccagcc ttgtagcccc cttcccctta gggggcctcc ttcaggaagc ccccgtcccc 540 tgcctccttg tggccacggt gacaccggaa cacttcagag gggcggctgg ggagttgggg 600 tgggacgggc tctcccgcag ctggagccgg tgtgtgacgc gggaacgcgg ccaagcgcgc 660 cccatccagg cggcctatca ggagccgtcg tcggacaatg gctccgcgcc tgacaacccc 720 gtcgtccccg tgccgtcccc cgaactccac ataccatgcg acgcgcggcc agccccccgc 780 ccctgcccgg ctgctgggag gaagtgacag cgccccgcat cccccgctgg gcaggccggg 840 cgcgcccagc ccctgggacg cagggacaca gccgggccgc gctgggcctt ggcctccgcc 900 cgcgggtttt ccgcggttgc ggcggggcgg ggaaggaggg gcgggcgggg cggggctgac 960 tctgcgacta tttcaggcct tgcggaaccc gggccaggac agtggcggcc aggccgggac 1020 acggtaagtg acctccgctt ccacacgtcc attccccgcc gctccgcgcg gcttctcgcc 1080 cgcccctacc ccgaggccag 1100 // ID HSA_7128_TNFAIP3 standard; DNA; HUM; 1100 BP. XX AC 7128; XX DT 06-Sep-2005 (Created) XX DE TNFAIP3: tumor necrosis factor, alpha-induced protein 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 138229089..138230188 (FORWARD) CC Score Points: 5 (38.5%) CC Chromosomal Location: 6q23 XX CC Database Reference HGNC: 11896; TNFAIP3 CC Database Reference ENTREZGENE: 7128 CC Database Reference UNIGENE: Hs.211600 CC Database Reference ENSEMBL: ENSG00000118503 CC Database Reference REFSEQ: NM_006290 CC Database Reference REFSEQ: NP_006281 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202643_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202643_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202644_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202644_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202643_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202644_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:595_at CC Database Reference TRANSFAC GENE: G000265; A20 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 138229089..138230188" FT /note="Genomic Strand: FORWARD" FT misc_feature 958 FT /note="SECONDARY ANCHOR: MMU [21929]; Alignment" FT prim_transcript 971..>971 FT /db_xref="dbTSS:FMR01186" FT /note="Number of reported TSSs: 2" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:KGR00786" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:SMR07777" FT prim_transcript 1063..>1063 FT /db_xref="ENSEMBL:ENST00000237289" XX SQ Sequence 1100 BP; 227 A; 326 C; 346 G; 201 T; 0 other; cacctgcacc cccactgccc agggggctgc atccatctcc acatgactca ccctccctgt 60 gcaacgcatg ggggtaggga gggaagcgcc agtattatca gccatcagca ccctggggtg 120 aactgattat caggacaact aaaaacacac ctaataaagc cttggagaca catggcaagc 180 accgtgatgg actagaagcg atttctaagc tgaaatgctg ctttgaatgc aatgtcagct 240 ggatgcttgg tgagcagaaa tagacaaggg gaaatggagc aagcgcggca taggggtgag 300 tgttgttctg attcctaagt ttacctaaga ctggggccac ggggtcgggt gtcccctggg 360 acctacgtct catgcagcct ggggtccaga gctggcagga acaatggaga tggggaccaa 420 aggctgtcac cgctgctttt tctcgaaatg cccgcccggg tcctgtctgg ggctcccgcc 480 tacgcgctca tcacgtgcac agcccaaact tttcagagcc ggcccgaggc ctgcgggccc 540 gggcgccagg gtggttttta gggttttctt tctttcttat ttcccttctt cttctccaca 600 gttgatgatt ttctgcagaa aaacaactgc gaaaaagaac ctatttcatt tccagttccc 660 atcaccgcga tttccacatg gatgtgacgt gaccccagct tccgaaatgc ccaggtgact 720 cacgcgggga caccccgggg cggggcgagg gagtttctcc gggcgcctgc agggaccggg 780 cggggcgggg cagcggggcg gggcagggaa agggggcggg gcggggcccg caggcccggt 840 cgggcggagg ccgcgcgcgc ccctcgcccc ctgcgccctc tggcggccgg ctggacgcac 900 ttcgcagccc gacccagaga gtcacgtgac tttggaaagt cccgtggaaa tccccgggcc 960 tacaacccgc atacaactga aacggggcaa agcagactgc gcagtctgca gtcttcgtgg 1020 cgggccaagc gagcttggag cccgcggggg cggagcggtg agagcggccg ccaagagaga 1080 tcacaccccc agccgaccct 1100 // ID HSA_7185_TRAF1 standard; DNA; HUM; 1100 BP. XX AC 7185; XX DT 05-Sep-2005 (Created) XX DE TRAF1: TNF receptor-associated factor 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.9 120770502..120771601 (REVERSE) CC Score Points: 1 (14.3%) CC Chromosomal Location: 9q33-q34 XX CC Database Reference HGNC: 12031; TRAF1 CC Database Reference ENTREZGENE: 7185 CC Database Reference UNIGENE: Hs.531251 CC Database Reference ENSEMBL: ENSG00000056558 CC Database Reference REFSEQ: NP_005649 CC Database Reference REFSEQ: NM_005658 CC Database Reference AFFYMETRIX: AFFY_HG_U95E:74382_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:74384_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:76878_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:849_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205599_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205599_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205599_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:90942_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:235116_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:235116_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:848_at CC Database Reference TRANSFAC GENE: G006839; TRAF1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="9" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 120770502..120771601" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000317379" XX SQ Sequence 1100 BP; 184 A; 366 C; 339 G; 211 T; 0 other; agttccataa ctattttgat taatatattc ttaaggattt agcgaccgtg tgtgtgtgtg 60 tttagacgaa aacagaaacg gttccttaaa atatccagtt tgtaaaagca cagtgccttg 120 aaccacttag tactatcatt ttgatcaagt actatcaagt actatcactt gattgctcca 180 acccaataag cttgggcgag cctggcactg tgctaggatc ttctggagaa atccaagaaa 240 ggtaagactg cggttttact cctcttcacc ttctcactac tcggattttg ggcaggcagg 300 ggaccagggt gggggctcca attcccggtt tgtgtttgtt ttttcagggg gcatcttact 360 gagcactaaa cacgcgcagg tgctgcacca gatgccagga gccccgcaag cggaggagct 420 gcgtacacgc gtgtcagtta actgggcgca cagtgcccgt ggcgccgcag acccggccct 480 cagactcagt ttcccctcac agggatcgct cgccccgccc cgcggcggtc tggggagcag 540 cagccccggg ccccggccct gccttgccgg tttccgccgg tgcggctgcg tccttcacac 600 tccaccggaa gctccgggcc tggccgccgg taggcggtgg cggaggcggc gccgaggttg 660 gctgccctac acccctgccc cgggaccgca gggcggctcc ccggccccct tcctcgcccc 720 gaactccccg ctccagctcc cgcttgctga ggcggggact cctcgggtgc agccggggac 780 ctggcacctc ggctgcagag accgccccgg actcaactgc ccccagccca gccgcgggcg 840 ccccggcccc gcaggggctc attcctcttt ccgcgggcac cggcgctgcc tggctcccag 900 cgctgccctc gcaactggat atgtggaggt ggcgacgcga cactcccccg ccctcgggcg 960 ggctcaccga cctggctggg ggctcagcct gcagagccgg gcggcggggg ctgtgctggc 1020 gccggcaggc gcgaggaatc acagagcggg gcgcccagcc tcatcatggg gcggcccacg 1080 gagacttccc gtgggagtgg 1100 // ID HSA_7412_VCAM1 standard; DNA; HUM; 1100 BP. XX AC 7412; XX DT 06-Sep-2005 (Created) XX DE VCAM1: vascular cell adhesion molecule 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 100896318..100897417 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 1p32-p31 XX CC Database Reference HGNC: 12663; VCAM1 CC Database Reference ENTREZGENE: 7412 CC Database Reference UNIGENE: Hs.109225 CC Database Reference ENSEMBL: ENSG00000162692 CC Database Reference REFSEQ: NP_001069 CC Database Reference REFSEQ: NM_080682 CC Database Reference REFSEQ: NM_001078 CC Database Reference REFSEQ: NP_542413 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203868_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41433_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:583_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203868_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203868_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:85611_r_at CC Database Reference TRANSFAC GENE: G001070; VCAM-1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 100896318..100897417" FT /note="Genomic Strand: FORWARD" FT misc_feature 879 FT /note="SECONDARY ANCHOR: MMU [22329]; Alignment" FT misc_signal 925..949 FT /note="TRANSFAC Site R13476" FT /note="TRANSFAC Site R13477" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000294728" FT /note="Number of reported TSSs: 2" FT misc_feature 1044 FT /note="SECONDARY ANCHOR: RNO [25361]; Alignment" XX SQ Sequence 1100 BP; 321 A; 216 C; 203 G; 360 T; 0 other; acctgcacgt gtttaataaa aggaagtggc tattccggtt tctttttgat gggcaagcat 60 tttgcaaggc cttgggctat gtgtgtgcaa ggctaagcca gttagttaat tgggattttt 120 ttaaaaaggc acttcactgg ggggaaaagg aacatagagt tggttattgt ccccttgcct 180 ataataaaaa cctattattt ttaatttttt aactgggttt gcggttaaat ctcacagccc 240 aagagatttg ccacttcaga tggattccat acacttgcat ttaagtatgc aaaaaaattc 300 caattatcca gcaatttaac caaattattg gtaacttttc taaaacaaaa aaaaattgtt 360 tcccttgttt tggcagcaat ttcagttaca gtcctttact ttctactcaa gaaaatagtt 420 tcaaaaagtt gatgtttgtt gctaaaagaa ctatttttat gaataaatat aaaactaaga 480 agttatggtg tccctttttt aaaaaatgac tcatcaaaag aaataacttt ttcctttctc 540 ttgtaagaga aaaaaattaa tctcttttag aattgcaaac atatttcctt gatggagaaa 600 atcaattcac atggcatagt cgttatttat ccagttcaaa aaccagagta gaatttacta 660 ctctgtctcc attttttctc tccccacccc cttaacccac attggattca gaaagcttca 720 ttctgcaatc agcattgtcc tttatctttc cagtaaagat agccttttgg agtcgaagat 780 gaggaaaagc ctgtatttta tagtcttgga agtgtcttct tttgccagga cagagagagg 840 agcttcagca gtgagagcaa ctgaaggggt taatagtgga acttggctgg gtgtctgtta 900 aacttttttc cctggctctg ccctgggttt ccccttgaag ggatttccct ccgcctctgc 960 aacaagaccc tttataaagc acagactttc tatttcactc cgcggtatct gcatcgggcc 1020 tcactggctt caggagctga ataccctccc aggcacacac aggtgggaca caaataaggg 1080 ttttggaacc actattttct 1100 // ID HSA_7422_VEGF standard; DNA; HUM; 1100 BP. XX AC 7422; XX DT 06-Sep-2005 (Created) XX DE VEGF: vascular endothelial growth factor XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 43844979..43846078 (FORWARD) CC Score Points: 4 (57.1%) CC Chromosomal Location: 6p12 XX CC Database Reference HGNC: 12680; VEGF CC Database Reference ENTREZGENE: 7422 CC Database Reference UNIGENE: Hs.73793 CC Database Reference ENSEMBL: ENSG00000112715 CC Database Reference REFSEQ: NP_001020539 CC Database Reference REFSEQ: NM_003376 CC Database Reference REFSEQ: NP_001020540 CC Database Reference REFSEQ: NP_003367 CC Database Reference REFSEQ: NM_001025370 CC Database Reference REFSEQ: NP_001020537 CC Database Reference REFSEQ: NM_001025366 CC Database Reference REFSEQ: NM_001025369 CC Database Reference REFSEQ: NM_001025367 CC Database Reference REFSEQ: NM_001025368 CC Database Reference REFSEQ: NP_001020538 CC Database Reference REFSEQ: NP_001020541 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211527_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211527_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210512_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210513_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210513_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212171_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210513_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210512_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36100_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212171_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1953_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211527_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212171_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210512_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:73146_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36101_s_at CC Database Reference TRANSFAC GENE: G002597; VEGF XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="6" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 43844979..43846078" FT /note="Genomic Strand: FORWARD" FT prim_transcript 946..>946 FT /db_xref="ENSEMBL:ENST00000324450" FT prim_transcript 948..>948 FT /db_xref="ENSEMBL:ENST00000356655" FT /db_xref="dbTSS:KDN02145" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [83785]; Alignment" XX SQ Sequence 1100 BP; 179 A; 338 C; 359 G; 224 T; 0 other; ccagtcactg actaaccccg gaaccacaca gcttcccgtt ctcagctcca caaacttggt 60 gccaaattct tctcccctgg gaagcatccc tggacacttc ccaaaggacc ccagtcactc 120 cagcctgttg gctgccgctc actttgatgt ctgcaggcca gatgagggct ccagatggca 180 cattgtcaga gggacacact gtggcccctg tgcccagccc tgggctctct gtacatgaag 240 caactccagt cccaaatatg tagctgtttg ggaggtcaga aatagggggt ccaggagcaa 300 actcccccca ccccctttcc aaagcccatt ccctctttag ccagagccgg ggtgtgcaga 360 cggcagtcac tagggggcgc tcggccacca cagggaagct gggtgaatgg agcgagcagc 420 gtcttcgaga gtgaggacgt gtgtgtctgt gtgggtgagt gagtgtgtgc gtgtggggtt 480 gagggcgttg gagcggggag aaggccaggg gtcactccag gattccaata gatctgtgtg 540 tccctctccc cacccgtccc tgtccggctc tccgccttcc cctgccccct tcaatattcc 600 tagcaaagag ggaacggctc tcaggccctg tccgcacgta acctcacttt cctgctccct 660 cctcgccaat gccccgcggg cgcgtgtctc tggacagagt ttccgggggc ggatgggtaa 720 ttttcaggct gtgaaccttg gtgggggtcg agcttcccct tcattgcggc gggctgcggg 780 ccaggcttca ctgagcgtcc gcagagcccg ggcccgagcc gcgtgtggaa gggctgaggc 840 tcgcctgtcc ccgccccccg gggcgggccg ggggcggggt cccggcgggg cggagccatg 900 cgcccccccc tttttttttt aaaagtcggc tggtagcggg gaggatcgcg gaggcttggg 960 gcagccgggt agctcggagg tcgtggcgct gggggctagc accagcgctc tgtcgggagg 1020 cgcagcggtt aggtggaccg gtcagcggac tcaccggcca gggcgctcgg tgctggaatt 1080 tgatattcat tgatccgggt 1100 // ID HSA_767_CA8 standard; DNA; HUM; 1100 BP. XX AC 767; XX DT 06-Sep-2005 (Created) XX DE CA8: carbonic anhydrase VIII XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 61356409..61357508 (REVERSE) CC Score Points: 2 (100.0%) CC Chromosomal Location: 8q11-q12 XX CC Database Reference HGNC: 1382; CA8 CC Database Reference ENTREZGENE: 767 CC Database Reference UNIGENE: Hs.491813 CC Database Reference ENSEMBL: ENSG00000178538 CC Database Reference REFSEQ: NP_004047 CC Database Reference REFSEQ: NM_004056 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:220234_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:49724_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:238537_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:68909_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:238537_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:220234_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:220234_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 61356409..61357508" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000317995" FT /db_xref="dbTSS:KMR06540" XX SQ Sequence 1100 BP; 269 A; 295 C; 281 G; 255 T; 0 other; aaaacaaatt gtacttaagg tcctaactcg agtttattgt gcacatatat cttctaaaaa 60 tgtggagtta acctacttag gggttactga ccagggcttt taaaaggcac aggaacagag 120 ggctgaagtc gttaacacta gactgagaag cacgtttaag ggtaacaatg ccacctcttt 180 ggatcagaag agttcctgtt tgttatgcaa tgtgtgcact tcattattta cacgatttca 240 ctaggtgaat gggagctgtg tacacagcca ggtgagcctg cagcagcgcc ccagactctg 300 acagcgaaca ccctctgtct actgccttct gctagccctg ctttgaaaca ataccctttt 360 ctggaaaaaa aaaaaaaaaa aacacaaccc taaatcatag ctacttctct agataacaac 420 cattttcttt tcttaaacgt ttttaggaat taatagaact ttcttggaaa aatttccaaa 480 ctcgtttcca ctgcgctgaa cggacgattt aaaaagtaaa tactcagaag atactaagaa 540 gattccgctg gagagtctct ttttattgtg ttacggggtc tcctagccct ctcctttctc 600 ctacccacgg cagcccatct ctctcctcca ggaccccttc tttttggtat ttcctggagt 660 acggatgaaa atgaataggt gagcagcctc tgggctaggc caggcacaca ggggtcccga 720 gtgaccttgg gagacttgcg ggcttctgga aggaaggctc gggcggccaa gcaggagtcg 780 ccgcagcgag gaagcgccag gaggcggcgg gggcgacccc gggggaaggg cgggcgggga 840 tgcgccgagg tttccgtgac ttgggactag tcgccccgag gcgcattcta actgtcggct 900 cccctggccc caacggccag agagagaagg gggcggatcc tcgcgtacca gacacgcccc 960 ggtcgggtat aaaattcgcc aggcgctcgc tccccaggcc acagccgctc cctcgctctg 1020 ctggggcctc cggacgcgct tcccacgcgg gtctctggaa cactcggtcc gaacgcacgc 1080 ctgcttgcac tcacactgcg 1100 // ID HSA_79155_TNIP2 standard; DNA; HUM; 1100 BP. XX AC 79155; XX DT 07-Sep-2005 (Created) XX DE TNIP2: TNFAIP3 interacting protein 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 2795210..2796309 (REVERSE) CC Score Points: 1 (50.0%) CC Chromosomal Location: 4p16.3 XX CC Database Reference HGNC: 19118; TNIP2 CC Database Reference ENTREZGENE: 79155 CC Database Reference UNIGENE: Hs.368551 CC Database Reference ENSEMBL: ENSG00000168884 CC Database Reference REFSEQ: NM_024309 CC Database Reference REFSEQ: NP_077285 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:218335_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:232160_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:48531_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:232160_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:218335_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:48531_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:48531_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:218335_x_at CC Database Reference TRANSFAC GENE: G004862; TNIP2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="4" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 2795210..2796309" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000315423" XX SQ Sequence 1100 BP; 221 A; 279 C; 415 G; 185 T; 0 other; aacactagcg tttgtctggg aattttgggg aaggaaaggg atggaaaagc gaaagggtgg 60 gaaggggctg gtttcctgct gcttctgcta tataagaaca gcatctagca ggaaggttgt 120 cccgtgggcc catactagcc accttacaaa gcagcgtctg cagtggctga cgcctgtaat 180 cccagcactt tgggaggctg aggccggtgg atctacctga ggtcaggagt tcaagaccag 240 cctggccaac atggtgaaac accatctcta ctaataatac caaaaaatta gcagggcatg 300 gtggcgggcg cctgtaatcc cagctactca ggaggctgag gcaggagaat cgcttgaaac 360 tgggaggcgg aggttgtagt gagccgagat cgcgccatta cactccagcc tgggcaacag 420 agcgaaactc cgtctcaaaa agaagaaaaa aaaggaaaga aaaaagaaag cggcgtgcgg 480 ggcagggggt tggagctctt tctgggctca gtgtccccag gtgacggaac acatgccacg 540 tgcttggtgc gctgcgagct cagctcctgg agcttctgtt gctgctgtgg ccgcaaggcc 600 tggaccctcg cggggagatt cagacccaca cttagctcca gagcttgggg gttgtcgtta 660 agcccttcct ttccatcaga ggctgatgaa tccccaaact cctgggctga gttcgactct 720 ccgacaactc ctcagaggcg gatgtttggg gccactggaa taagcccagc accagctggg 780 gtgtggacag cctcgggggc caggccaact ctcccggacg ggtgcggacg gcaggggcgg 840 ggccgggctg taggcggtgg gaggggtggg gccgggcgag aaggggctgg gcgggctgcc 900 gtcgggcggg gctgcgcggg gaagggcggg gctgcgcggg gggcggggct gcgtggggga 960 gggcggggcc gggctgttgt gggtgggcgg ggcgcaccgg ggaaagttcc gggaagggcg 1020 gcagccggcg gggcccgggc gcggaagttg ccggcggccg cgcggcctcc cgggcgggcc 1080 tacagccatg tcccgggacc 1100 // ID HSA_80223_RAB11FIP1 standard; DNA; HUM; 1100 BP. XX AC 80223; XX DT 07-Sep-2005 (Created) XX DE RAB11FIP1: RAB11 family interacting protein 1 (class I) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 37876055..37877154 (REVERSE) CC Score Points: 6 (85.7%) CC Chromosomal Location: 8p11.22 XX CC Database Reference HGNC: 30265; RAB11FIP1 CC Database Reference ENTREZGENE: 80223 CC Database Reference UNIGENE: Hs.191179 CC Database Reference ENSEMBL: ENSG00000156675 CC Database Reference REFSEQ: NP_001002233 CC Database Reference REFSEQ: NM_001002233 CC Database Reference REFSEQ: NM_025151 CC Database Reference REFSEQ: NP_001002814 CC Database Reference REFSEQ: NP_079427 CC Database Reference REFSEQ: NM_001002814 CC Database Reference AFFYMETRIX: AFFY_HG_U95E:89338_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:57608_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219681_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:231830_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:225177_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219681_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:231830_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:225177_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219681_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:92071_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:55686_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 37876055..37877154" FT /note="Genomic Strand: REVERSE" FT prim_transcript 982..>982 FT /db_xref="dbTSS:STM06182" FT /note="Number of reported TSSs: 2" FT prim_transcript 985..>985 FT /db_xref="dbTSS:KMR05673" FT prim_transcript 994..>994 FT /db_xref="ENSEMBL:ENST00000287263" FT prim_transcript 1025..>1025 FT /db_xref="ENSEMBL:ENST00000330843" FT prim_transcript 1038..>1038 FT /db_xref="ENSEMBL:ENST00000343853" XX SQ Sequence 1100 BP; 189 A; 335 C; 330 G; 246 T; 0 other; ggagggcaaa ataggacact cccacattga actcatgctc cccaggatac cttccccttt 60 tccggccctc acaaggtcct caccttcctc tgcagctgcc ttcctccaga gcaaggcttt 120 ccagcgggag aagtagaaag cacagtgaat tgggtgggca tcttccttag caccctcata 180 gttaccaact ttattttttt gagacagggt cttgctctgt tgcccaggct gggagtgcag 240 tggcacgatc tcggctcact gcacctcgac ctcctgggct ccagagatcc tccagactca 300 gcctcccaag tagcggggac cacaggcgct tgccaccact cctatctaat tatttttaat 360 tttttttgta gagacgggga tctggctatg ttgcccaggc tggtctcgaa ctcctgggct 420 caggagatcc tcctgtctca gcctcccaac gtgctggtca tggttattta ctgagaactc 480 accatgagcc aggcactggg ccaagaactg taatgcatta ttattattat tttttacagc 540 aatcctagga ggtgattgtc aggtgaagaa attgagactt gatgttaggt aatccgcgca 600 aggccacgac tggcgatgtg accctggaaa tgaggtctga cttccaagtc agtgcttcgg 660 ccagctcctt cccgccgtgc gacctttggc agctggggac cccatccgtc acctaccacc 720 tctcagatta gattctcgat gcgcccgccc ctgcgcacgt gatcccctgc ctgcctggcc 780 gcgccagccc cgcctccggc gcccgggtgc ccggagctgc ccgcgctgct gaggccggcg 840 gggcggggcg gggcggggcg gggcgcggcg cagcaggtgg agcaggcggc tcgggcaggg 900 gcgtggcctt ggccatgagg ggcgtggcct ggcgggggtg tggccggaag ccttaaagtg 960 gcctggtcgc cggggcgggc cgtggaggcc gccagtcgcg gcgatcttct cctcgcttct 1020 ggagtgttat cgtcaccatg tccctaatgg tctcggctgg ccggggcctg ggggccgtgt 1080 ggtccccaac ccacgtgcag 1100 // ID HSA_80833_APOL3 standard; DNA; HUM; 1100 BP. XX AC 80833; XX DT 06-Sep-2005 (Created) XX DE APOL3: apolipoprotein L, 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.22 34881212..34882311 (REVERSE) CC Score Points: 53 (96.4%) CC Chromosomal Location: 22q13.1 XX CC Database Reference HGNC: 14868; APOL3 CC Database Reference ENTREZGENE: 80833 CC Database Reference UNIGENE: Hs.474737 CC Database Reference ENSEMBL: ENSG00000128284 CC Database Reference REFSEQ: NM_145639 CC Database Reference REFSEQ: NM_145642 CC Database Reference REFSEQ: NP_055164 CC Database Reference REFSEQ: NM_014349 CC Database Reference REFSEQ: NP_663617 CC Database Reference REFSEQ: NP_663615 CC Database Reference REFSEQ: NM_145641 CC Database Reference REFSEQ: NP_085147 CC Database Reference REFSEQ: NM_145640 CC Database Reference REFSEQ: NP_663616 CC Database Reference REFSEQ: NM_030644 CC Database Reference REFSEQ: NP_663614 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:221087_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:80945_f_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:50297_f_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:50296_i_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:221087_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:221087_s_at CC Database Reference TRANSFAC GENE: G018561; APOL3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="22" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 34881212..34882311" FT /note="Genomic Strand: REVERSE" FT misc_feature 596..622 FT /note="ChIP-on-Chip Fragment: cMyc" FT /note="PubMed:14980218" FT prim_transcript 835..>835 FT /db_xref="ENSEMBL:ENST00000337769" FT /note="Number of reported TSSs: 3" FT prim_transcript 1009..>1009 FT /db_xref="EPD:EP73070" XX SQ Sequence 1100 BP; 280 A; 241 C; 316 G; 263 T; 0 other; tcttcctaat atactctttt gtctttgtct tttactccca catccgcccc ccactttgtt 60 cagtcaacct gggactgtgg ccaattacaa cagcctaaca aaagtgccac aggagtggaa 120 catggggcag tgggctctgc tgaagaggat gctagggggc ttctcagggg aggaaatgct 180 agatttgcat tctgatagag gagcgtgact tttccaggtg aaggtagcag gtgctcctgg 240 cagaagaacc cacataagga agtgtccaga agccacacag gtatggcgtt cgacaagagc 300 aggtctggaa cggtggctca tgctgaggca ggaggatcat ttgaggccag agtttgaaac 360 caacctggta aaaatagtaa gatttcaccc cttcaaaatc attttttaaa agtagccagg 420 ccgagtggct catgcttgta gtcccagcta ctcaggaggt tcatttgaac cctggaattt 480 gaggctacag tgagctatta ttgtgccacc gcactccagc ctgggtgaca gagccagacc 540 ccatctcaaa aacaaaacaa aacaaaacaa caaaataacc ccaacagcaa tacaatcaat 600 atgcaataag cgtccacccg gcatgtgtga tggactgtgg taatgctgat ggcatggagg 660 gagtgaggtg ggcatctggg gagtgtggtg ttattggggg tggggagtaa tctggagggt 720 ctcatagtct ttcagtggta ggtctttctt cctgaagaca cagcaaaccc ccaaccctaa 780 gtatgggagg caggtgggtt ggccaagaag gacgtctggg gctgctcttg gatcagcagg 840 agggtgggac caagggtgct gctggaccaa ggatgggact gggccaaggg tggggctggg 900 aagcatcctg ttttgcatgt ttgatcagga gctgctgcca agttgtgact ttcactttcc 960 cttttgggtt ccagggtata tctcagagcc tggagaacgt gtctggttat tatgcagatg 1020 cacggctgga ggtgggatcc acacagctca gaacagctgg atcttgctca cactctttca 1080 agagaagctt ccttggtaag 1100 // ID HSA_81788_NUAK2 standard; DNA; HUM; 1100 BP. XX AC 81788; XX DT 07-Sep-2005 (Created) XX DE NUAK2: NUAK family, SNF1-like kinase, 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 202022441..202023540 (REVERSE) CC Score Points: 1 (50.0%) CC Chromosomal Location: 1q32.1 XX CC Database Reference HGNC: 29558; NUAK2 CC Database Reference ENTREZGENE: 81788 CC Database Reference UNIGENE: Hs.497512 CC Database Reference ENSEMBL: ENSG00000163545 CC Database Reference REFSEQ: NM_030952 CC Database Reference REFSEQ: NP_112214 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:220987_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:220987_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:220987_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:55353_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:92066_at CC Database Reference TRANSFAC GENE: G009469; SNARK XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 202022441..202023540" FT /note="Genomic Strand: REVERSE" FT misc_feature 418..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF6_hep" FT /note="PubMed:14988562" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000295786" XX SQ Sequence 1100 BP; 246 A; 307 C; 283 G; 264 T; 0 other; ccattttcag acttagggac acaggttaga tagtcggcat gtaaaaatgt taaataaata 60 tgtatccctt cgggttctct ccacctccag ccgacacatc ctaaataaat tccactaagt 120 ggttgaggga atctactaaa ccttagaagc cctctttttt tttgaaacgg agcctcactt 180 tgttgcccag gctggagtgc agtggcgcca tcttgattca ctgaaacctc tgcctcctgg 240 gttcaagcga ttcttctgcc tcagcctcca gagtagctgg gattacaagc gcgcaccacc 300 acgcccggct aattttgtat ctttagtgga gatgggattt cgtcatgttg gctaggttgg 360 tcttgaactc ctggacctca agcgattcgc ctaagaagcc ctctttgagg aagaaggaag 420 aagtttccag ggccattgga ttccaatatc caagtaaggt tgatctaact gaagacaagt 480 gaactcgaac cataggacag ctctgcacta accctcccac taggctggat tctgcctctg 540 ttccatccca gctccctttc tcctttatgg actcaatgaa gtggtcaagc aattatagat 600 tttggcttgg gacaagcaaa ttactcagga tgaagaaata ctttggtgac ctttagtgcc 660 ctcagatcgc cccttgccaa ctgagaacag agtacaataa aacaacaggg cattaagcag 720 gaccaagcgc cactcagagg caagtgcagc tccaagggcc ctcagagtaa gcttctgggc 780 ctcaggcggc cttcgctgga atcccctagt ccccattcct ggtgggcggg ttccattgac 840 acctttcccg gccacgccga gggggaggag gcggggcctg gagccccgga gagccaatgt 900 ggacggccgt ggtcacgcgc cgccgtcgag caggccaatg ggcgccgggg ggcgtgtcca 960 gggcctcggg ctcagggcgt ttataacaac ttggaatgct gtgctttact gcgcgctctg 1020 gtactgctgt ggctccccgt cctggtgcgg gacctgtgcc ccgcgcttca gccctccccg 1080 cacagcctac tgattcccct 1100 // ID HSA_8204_1_NRIP1 standard; DNA; HUM; 1100 BP. XX AC 8204_1; XX DT 07-Sep-2005 (Created) XX DE NRIP1: nuclear receptor interacting protein 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.21 15257172..15258271 (REVERSE) CC Score Points: 4 (15.4%) CC Chromosomal Location: 21q11.2 XX CC Database Reference HGNC: 8001; NRIP1 CC Database Reference ENTREZGENE: 8204 CC Database Reference UNIGENE: Hs.155017 CC Database Reference ENSEMBL: ENSG00000180530 CC Database Reference REFSEQ: NM_003489 CC Database Reference REFSEQ: NP_003480 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202600_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202600_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202600_s_at CC Database Reference TRANSFAC GENE: G005148; NRIP1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="21" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 15257172..15258271" FT /note="Genomic Strand: REVERSE" FT prim_transcript 173..>173 FT /db_xref="dbTSS:KGR06385" FT prim_transcript 696..>696 FT /db_xref="dbTSS:COL01722" FT prim_transcript 997..>997 FT /db_xref="dbTSS:COL04055" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:COL08056" XX SQ Sequence 1100 BP; 359 A; 199 C; 187 G; 355 T; 0 other; gctacttagt aaaaattgat tacaattgag ggaagtttga tagatccttt aaaaaaaagg 60 cagatttcca ttttttgtat tttaactact ttactaaatt aatactcctc cttttacaga 120 attagaaaag ttaacattta tctttaggtg gtttcctgaa aagttgaata tttaagaaat 180 tgtttttaac agaagcaaaa tggcttttct ttggacagtt ttcaccatct cttgtaaaag 240 ttaattctca ccattcctgt ggtacctgcg agtgttatga ccaggattcc ttaaacctga 300 actcagacca cttgcattag aaccatctgg agcacttgtt ttaaaatgca gattcatagg 360 cagcatctca gatctacaga acaagaatct ctgctaagtg gacctggaat cttccatctg 420 catcttaaca tgctctctag gtgtttcttg tgtttgagaa ccatgactta tgactttcct 480 cagaacatga gactgtaaaa caaaaacaaa aaactatgtg atgcctctat tttccccaat 540 acagtcacac atcagctcaa aatttgcaat attgtagttc atatattacc gttatgtctt 600 tggaaatcgg gttcagaaca ctttttatga caaaaattgg gtggagggga taactttcat 660 atctggctca acatctcagg aaaatctgtg attatttgtg tgttctaatg agtaacatct 720 acttagttag ccttagggat ggaaaaacag ggccacttac caaactcagg tgattccagg 780 atggtttgga aacttctcct gaatgcatcc ttaaccttta ttaaaaccat tgtcctaaga 840 acaatgccaa caaagcttac aacatttagt ttaaacccaa gaagggcact aaactcagat 900 tgactaaata aaaagtacaa agggcacata tacgtgacag aattgtacac aatcactcca 960 ttggatcttt tactttaaag tagtgatgaa aagtacatgt tgatactgtc ttagaagaaa 1020 ttaatatatt agtgaagcca catggggttt cagttgcgaa acaggtctgt ttttatgttc 1080 agtttgtaca atccacaatt 1100 // ID HSA_8553_BHLHB2 standard; DNA; HUM; 1100 BP. XX AC 8553; XX DT 06-Sep-2005 (Created) XX DE BHLHB2: basic helix-loop-helix domain containing, class B, 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.3 4995148..4996247 (FORWARD) CC Score Points: 13 (81.2%) CC Chromosomal Location: 3p26 XX CC Database Reference HGNC: 1046; BHLHB2 CC Database Reference ENTREZGENE: 8553 CC Database Reference UNIGENE: Hs.171825 CC Database Reference REFSEQ: NM_003670 CC Database Reference REFSEQ: NP_003661 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201169_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201170_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201169_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40790_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201170_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201170_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201169_s_at CC Database Reference TRANSFAC GENE: G009148; BHLHB2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="3" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 4995148..4996247" FT /note="Genomic Strand: FORWARD" FT misc_feature <1..720 FT /note="ChIP-on-Chip Fragment: HNF1a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT misc_signal 794..823 FT /note="TRANSFAC Site R14551" FT misc_feature 942 FT /note="SECONDARY ANCHOR: RNO [79431]; Alignment" FT prim_transcript 973..>973 FT /db_xref="dbTSS:KDN02237" FT prim_transcript 975..>975 FT /db_xref="dbTSS:TDR04217" FT /note="Number of reported TSSs: 3" FT misc_feature 975 FT /note="SECONDARY ANCHOR: MMU [20893]; Alignment" FT prim_transcript 979..>979 FT /db_xref="dbTSS:KGR05592" FT /note="Number of reported TSSs: 2" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:HPR01174" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:HCR01476" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [79431]; Alignment" FT prim_transcript 1010..>1010 FT /db_xref="dbTSS:HRC01119" FT prim_transcript 1014..>1014 FT /db_xref="dbTSS:PRS00183" FT prim_transcript 1017..>1017 FT /db_xref="dbTSS:KMR09527" FT prim_transcript 1050..>1050 FT /db_xref="dbTSS:KGR03871" FT prim_transcript 1061..>1061 FT /db_xref="ENSEMBL:ENST00000256495" XX SQ Sequence 1100 BP; 165 A; 427 C; 349 G; 159 T; 0 other; agcgcccggt atctttctgc gcttgactgg ccgggaggaa gggggtgaca ctggggcacc 60 cagggggctg cgcaaccggg tgcccgcccg cccgcaggtt gtgcccagga gcggagctcc 120 tgggagcgag gggccctcgg ctcacaccct ccacggtcag gtgcgcgcgg cgtgctcggc 180 ggcagcctca gctgcccctg cgcttggccg tcggcccgct tcccatgggg tgacatccgc 240 cccgcccctc ggtccctccc caaggcgggc aattcctgga cgcgagggtg agcagtgggg 300 gcagggaagc caggacggaa agaaacccca gcctctgggg aaggctgggg ggccgggcga 360 ctccctccgc agcgcgccgg ttcctccaag cgggccgggc gggggaggag gaagagggct 420 gggctggagc tagcaagggg atattcctct cccggcttga gtcagacgcg ggcggatccg 480 tcctcccccg ttccctccca ggagacggga acttacttca tttccctggg gcaggttcgc 540 ccacgttacc aacttctccc cctcccccag cacccccgtc ccttccagct tccgcgcccc 600 ccacccaact gggcaggacc caggtcgtgc tgccaccccc tcttcgggga aaggcggccg 660 cagccgcaga cacctggggg ccggggctgg gggtgggggc tccctagcag ccgccggagc 720 gttgtccaac acgtgagact catgtgatga agccggggga gggcgggcag gtcgctcctt 780 ccctccccgg cagtggccag acgtgcctgg agtcacaggg tagaacacgt agctccaacc 840 cacccactcg ctcccattta acccagcccg cagcctctcc attactcctc ggcttgcccc 900 cccacccccc cactccgccc taaccgcccc cccctcaccc gctccctccc gcctccccgc 960 ccgccccact tctcattcac ttggctcgca cggcgcagac agaccgcgca gggagcacac 1020 accgccagtc tgtgcgctga gtcggagcca gaggccgcgg ggacaccggg ccatgcacgc 1080 ccccaactga agctgcatct 1100 // ID HSA_8605_PLA2G4C standard; DNA; HUM; 1100 BP. XX AC 8605; XX DT 06-Sep-2005 (Created) XX DE PLA2G4C: phospholipase A2, group IVC (cytosolic, calcium-independent) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.19 53305788..53306887 (REVERSE) CC Score Points: 13 (92.9%) CC Chromosomal Location: 19q13.3 XX CC Database Reference HGNC: 9037; PLA2G4C CC Database Reference ENTREZGENE: 8605 CC Database Reference UNIGENE: Hs.18858 CC Database Reference ENSEMBL: ENSG00000105499 CC Database Reference REFSEQ: NM_003706 CC Database Reference REFSEQ: NP_003697 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33707_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209785_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209785_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209785_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="19" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 53305788..53306887" FT /note="Genomic Strand: REVERSE" FT prim_transcript 970..>970 FT /db_xref="dbTSS:UBA09070" FT prim_transcript 990..>990 FT /db_xref="dbTSS:SYN02293" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:HPR01920" FT /note="Number of reported TSSs: 8" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:THR08279" FT prim_transcript 1016..>1016 FT /db_xref="dbTSS:SZR05473" FT prim_transcript 1023..>1023 FT /db_xref="ENSEMBL:ENST00000354276" XX SQ Sequence 1100 BP; 302 A; 265 C; 278 G; 255 T; 0 other; tgaaaccctg tctctactaa aaatacaaaa ataattagcc gggcgtggtg gcagatgcct 60 atgttcccag ctactcggga ggctgaggta ggagaatcgc ttgaacccag gagacggagg 120 ttgcagtgag ccgagattgc accactgcac accagcctgg gcgacaaaga gtaagactcc 180 atctcaaaaa aaaaaaaaaa aaattcaaaa cccatcgagt tgggatgacg cttagtgctg 240 ggcttcagga agagtaggca ggagggtagt atgggaggtt tctaggagcc actcttggaa 300 gcggtgctcc ccacagatgc ccgattgcac tgactggaac tcggtcacat gaccacataa 360 ctcgctcaca tgaccacacc tagctgcaaa ggtgctggga aatgtggtac cctgttggga 420 ggccacttct gggcttcaaa ccttcactgt gaatggagct cacaggtttt ctaaaaatgg 480 acattaaatg aaccagagtt ggccctaagg atctggctca ctgcaacctc cacctcccag 540 gatgaagcac ctgcctcagc ctcccgagta gtagctggga ttacaggcac acgccaccat 600 accgagctaa tttttgtatt tttagtagag aaggtgtttc accatgttgg ccaggctggt 660 ctcgaactcc tgacttcaca tgatccgcct gcctcagcct cccaaagtgc taggattaca 720 ggcgtaagcc accacgcctg gcctcaatat ttctttttct gggtatttga gtatgatatt 780 atatatgatg gttattagac agccagatgc ataggaggat tagctaatct gttttgagga 840 atacttatct ccaatatagt tatataacga caacattctt tttttgaata ctggtctcgg 900 gtgcctaatg acagaagggt gacatcacta aggaagcctg gaaagtccca gccctccacg 960 tgatcccacg gatgaaaata gctccgggtg agctctggaa cagctgaaaa agctggagca 1020 accaagcagg gcctacaagc cgaggagggc tgtttaaagg cgcaggggcc attttacctc 1080 caggttggcc ctgctcagga 1100 // ID HSA_8613_1_PPAP2B standard; DNA; HUM; 1100 BP. XX AC 8613_1; XX DT 06-Sep-2005 (Created) XX DE PPAP2B: phosphatidic acid phosphatase type 2B XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 56702119..56703218 (REVERSE) CC Score Points: 2 (5.7%) CC Chromosomal Location: 1pter-p22.1 XX CC Database Reference HGNC: 9229; PPAP2B CC Database Reference ENTREZGENE: 8613 CC Database Reference UNIGENE: Hs.405156 CC Database Reference ENSEMBL: ENSG00000162407 CC Database Reference REFSEQ: NP_803133 CC Database Reference REFSEQ: NM_003713 CC Database Reference REFSEQ: NP_003704 CC Database Reference REFSEQ: NM_177414 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212230_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209355_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212230_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:78684_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:78237_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33862_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209355_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209355_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212226_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212230_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212226_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212226_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 56702119..56703218" FT /note="Genomic Strand: REVERSE" FT prim_transcript 991..>991 FT /db_xref="dbTSS:MPC08759" FT prim_transcript 1011..>1011 FT /db_xref="dbTSS:PCD03787" XX SQ Sequence 1100 BP; 320 A; 231 C; 209 G; 340 T; 0 other; tgagcatcag gatttcgtga cataaagaat ataaaagcaa tgtctggtat ataataggta 60 atcagtaatt ggtggattat tttcagtagt gataaatctc ctctaagcat catatcatag 120 atacagtatg aaaatcaaga aagatttgag aaggatcgtc aggctcagag aagacagcac 180 aggctgactg gaggaaattc acaaacactg aagggcatcg tactacaagt ttcttagttg 240 ttagactggt attctattca tcacactctg cttctaaaaa gtaaaagcat cactttctgt 300 gatccaggtc atttcccatt catgttatcc tatttgaacc aacaactgca aaggtgagca 360 gcctcctttt atggagcaga aggccaaagc ttggaggatg tagattattg ctgaaggata 420 ccagattggt ggcagagtct gaattcccca ggacttaacc atggtgtgtc cagctcttct 480 tacagaaact ctcaccatgg ccaatgtcag cacaaggctg aggcccttac tagagtcagg 540 tcattgttgg tgatccttta ccccaaatct cagaatctcg agatttgctc agaccctgtg 600 acatcatagc taccctttac cttgtcgttg attcttcatt tagtatttct tttctatagt 660 taagttcttg tctctccctt aaaaaaaaag atacacacac acacacacac acacacacat 720 acacatatat acatataaat atatttggtt gtatattttt gttgttacaa aggggcttaa 780 aacacccaac tatattagcg ctttgatctt ttcttctgtg catatttgtg tctgtatatt 840 tcataaatag aaaattagga cactcctttg caaatactga atattctcct gtgttgttga 900 atatccgtta cggcatcagt gttgatgatg aatcttgata ctgcctaatt cccctgttgg 960 attcctttta gatcatcacg ggggaattct accggatcta ttacctgaag aagtcgcggt 1020 cgacgattca gaacccctac gtggcagcac tctataagca agtgggctgc ttcctctttg 1080 gctgtgccat cagccagtct 1100 // ID HSA_874_CBR3 standard; DNA; HUM; 1100 BP. XX AC 874; XX DT 05-Sep-2005 (Created) XX DE CBR3: carbonyl reductase 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.21 36428264..36429363 (FORWARD) CC Score Points: 2 (66.7%) CC Chromosomal Location: 21q22.2 XX CC Database Reference HGNC: 1549; CBR3 CC Database Reference ENTREZGENE: 874 CC Database Reference UNIGENE: Hs.154510 CC Database Reference ENSEMBL: ENSG00000159231 CC Database Reference REFSEQ: NP_001227 CC Database Reference REFSEQ: NM_001236 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205379_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205379_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38172_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205379_at CC Database Reference TRANSFAC GENE: G018318; CBR3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="21" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 36428264..36429363" FT /note="Genomic Strand: FORWARD" FT misc_feature 962 FT /note="SECONDARY ANCHOR: MMU [109857]; Alignment" FT prim_transcript 992..>992 FT /db_xref="dbTSS:KAT07762" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [109857]; Alignment" FT prim_transcript 1010..>1010 FT /db_xref="ENSEMBL:ENST00000290354" XX SQ Sequence 1100 BP; 279 A; 297 C; 287 G; 237 T; 0 other; ctcccaaagt gctgggatta caggtgtgag ccaccgcgcc cggaccaaat gatctttagg 60 agaaaaaaga aggaaatact gggggaggca cagtaggaga tcacagcagg ggcccacctc 120 cggaacctca agtaaggact tgagagagaa ggtagagtca gagtaacaga gacacaggcg 180 ggttagccag ctctgcatgg aaaaggctga gtcgtgatga tgtcatggtt ctccccaaat 240 ctcaaagtca ctgatcaaac aactcagttt acactgaaga cgatggatga gactctaatt 300 ttgtgcccac agcttgacac acctttggga atttggttta actttctttg ccggtacaca 360 gatctgtgag aacatatgat caatccagat ctttatagat ctatatcctc cctggacaaa 420 cctaaatgca gacactttta gcacccgtag gagttaggta ggattaaata aaaacattcc 480 ctcccacttg ggggcacatt cactgggaat cccagagcga tgtcgcctgc ccacacctgc 540 taagtgcgct cacagggcat ctagttccct ctcttgagtt ccttttaagc aagcaaggca 600 acctatgtcc agagaagcag ttactgtgtc taagtaagtc actgcatctt aggaaaaagc 660 aaacattcgc attttgcagt gcatgatggg cgcacaccca agaaaattac tcagcacttg 720 tttttctcac tttggggttt tcccaaaata atttcttcag tccagttgcc aagaatctgg 780 agcccccgac tgacccatca aggtccgatt tggcttcgga cacctcgcag atcaccccgc 840 ggctcagagc ccggatcctg aagggcgcag cgtgggcagg gggcgggccc gggagttgga 900 acagagggca cagacggccc ctcctcggag gggagggacc ggagccgggg cctttttctt 960 taagactcgc agcactggat cccagaactt agtctgcgcg gcggcattga cactagctgg 1020 gctcctcggg gcgcgcccca ggtggtccga agcccggtcc gccctccacg caggtgcccc 1080 gcgctccccg ctcagccatg 1100 // ID HSA_8743_TNFSF10 standard; DNA; HUM; 1100 BP. XX AC 8743; XX DT 06-Sep-2005 (Created) XX DE TNFSF10: tumor necrosis factor (ligand) superfamily, member 10 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.3 173723837..173724936 (REVERSE) CC Score Points: 94 (97.9%) CC Chromosomal Location: 3q26 XX CC Database Reference HGNC: 11925; TNFSF10 CC Database Reference ENTREZGENE: 8743 CC Database Reference UNIGENE: Hs.550091 CC Database Reference UNIGENE: Hs.478275 CC Database Reference ENSEMBL: ENSG00000121858 CC Database Reference REFSEQ: NP_003801 CC Database Reference REFSEQ: NM_003810 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1715_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202687_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202688_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202687_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:214329_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202688_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:214329_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:214329_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202687_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202688_at CC Database Reference TRANSFAC GENE: G006827; TNFSF10 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="3" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 173723837..173724936" FT /note="Genomic Strand: REVERSE" FT misc_feature 255..>1100 FT /note="ChIP-on-Chip Fragment: HNF6_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF6_panc" FT /note="PubMed:14988562" FT prim_transcript 942..>942 FT /db_xref="dbTSS:T3R00544" FT prim_transcript 964..>964 FT /db_xref="dbTSS:LNG15278" FT prim_transcript 966..>966 FT /db_xref="ENSEMBL:ENST00000241261" FT prim_transcript 969..>969 FT /db_xref="dbTSS:KAR09668" FT /note="Number of reported TSSs: 5" FT prim_transcript 970..>970 FT /db_xref="dbTSS:HRT04892" FT /note="Number of reported TSSs: 4" FT prim_transcript 974..>974 FT /db_xref="dbTSS:PRS08077" FT /note="Number of reported TSSs: 2" FT prim_transcript 975..>975 FT /db_xref="dbTSS:PRS00216" FT prim_transcript 978..>978 FT /db_xref="dbTSS:HSI06330" FT /note="Number of reported TSSs: 8" FT prim_transcript 980..>980 FT /db_xref="dbTSS:HRC05126" FT prim_transcript 984..>984 FT /db_xref="dbTSS:PLR04433" FT prim_transcript 1007..>1007 FT /db_xref="EPD:EP74583" FT prim_transcript 1012..>1012 FT /db_xref="dbTSS:REC00858" FT /note="Number of reported TSSs: 3" FT prim_transcript 1013..>1013 FT /db_xref="dbTSS:REC00727" FT /note="Number of reported TSSs: 2" FT prim_transcript 1015..>1015 FT /db_xref="dbTSS:HRC03660" FT /note="Number of reported TSSs: 6" FT prim_transcript 1016..>1016 FT /db_xref="dbTSS:NYUb0007.seq" FT prim_transcript 1038..>1038 FT /db_xref="dbTSS:HRC09039" FT prim_transcript 1039..>1039 FT /db_xref="dbTSS:HRC09019" FT prim_transcript 1045..>1045 FT /db_xref="dbTSS:HRC01749" FT /note="Number of reported TSSs: 4" FT prim_transcript 1048..>1048 FT /db_xref="dbTSS:T3R06008" XX SQ Sequence 1100 BP; 369 A; 193 C; 285 G; 253 T; 0 other; aaagaaagaa agaaagaaag aaagaaagaa agaaagaaag aaagaaagaa ggaaagaagg 60 aaagaataga aaagaaaaga aagaaagaaa gaaaggaaga aaaggaaaga aagaaatgct 120 gaataagata tagagacaac atacagctgg gccagcttat gacatctgat agtggggaga 180 tttggggctg ggtcctgaat ctgagggtaa ttaactccct gtaacttctt ttcctaatct 240 gtaaaaggat agtgacagcg agacattgtg atggggttaa tattttggaa aacatccaca 300 tgtttttttc ctttgccttt ctgagtgtgt caactacttc ctacctgtcc agcctaacac 360 acaggcatgt tgtcttggta gggatggaga tctgagaagg agattagaat ttgtgtctga 420 aggtttgcaa agaggaagaa gtcgtcaata tttagattct gacattcaag atggaattat 480 gtagcaagac cattgctatg agacagtatt tctattttcc tttatccact cccaccctgc 540 cctcttccca ccctcacagt agcatgagaa aaaccacata tggaagtttc aggtcataaa 600 aattatctta taatttagaa aacaggcctt gtgcctatga cagccaggcc atgaggctta 660 gagctctgtg gtagaatgag gatatgttag ggaaaagcaa agaaaatccc tcccctcttt 720 ggctgaggac attatcaaaa ggagagcaag aaagagaaga gagaaatggg cttgaggtga 780 gtgcagataa ggggtgcatg gatcctgagg gcaaggagag gagcttcttt cagtttccct 840 cctttccaac gactactttg agacaagagc tgtccctggg cagtaggaaa ggggagggac 900 agttgcaggt tcaatagatg tgggtggggc caaggccaca gaacccagaa aaacaactca 960 ttcgctttca tttcctcact gactataaaa gaatagagaa ggaagggctt cagtgaccgg 1020 ctgcctggct gacttacagc agtcagactc tgacaggatc atggctatga tggaggtcca 1080 ggggggaccc agcctgggac 1100 // ID HSA_8767_RIPK2 standard; DNA; HUM; 1100 BP. XX AC 8767; XX DT 06-Sep-2005 (Created) XX DE RIPK2: receptor-interacting serine-threonine kinase 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 90838196..90839295 (FORWARD) CC Score Points: 12 (92.3%) CC Chromosomal Location: 8q21 XX CC Database Reference HGNC: 10020; RIPK2 CC Database Reference ENTREZGENE: 8767 CC Database Reference UNIGENE: Hs.103755 CC Database Reference REFSEQ: NM_003821 CC Database Reference REFSEQ: NP_003812 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209544_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209545_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209545_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209544_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209545_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209544_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41384_at CC Database Reference TRANSFAC GENE: G003541; RIPK2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 90838196..90839295" FT /note="Genomic Strand: FORWARD" FT prim_transcript 963..>963 FT /db_xref="dbTSS:KAT07216" FT prim_transcript 978..>978 FT /db_xref="ENSEMBL:ENST00000220751" FT prim_transcript 982..>982 FT /db_xref="dbTSS:LNF04216" FT /note="Number of reported TSSs: 3" FT prim_transcript 984..>984 FT /db_xref="dbTSS:T3R06590" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:CAS03470" FT prim_transcript 1011..>1011 FT /db_xref="dbTSS:HRT03052" FT /note="Number of reported TSSs: 2" FT prim_transcript 1016..>1016 FT /db_xref="dbTSS:HCR08745" FT prim_transcript 1018..>1018 FT /db_xref="dbTSS:CAS01421" FT prim_transcript 1093..>1093 FT /db_xref="dbTSS:T3R07647" XX SQ Sequence 1100 BP; 263 A; 291 C; 329 G; 217 T; 0 other; tgaatcccta gaattaatta aacatctagt atggagttgg tattgtatat aacatttgca 60 ctcacgtctt acaaaatagt catctaagta gaaaggtatt caaggcagaa ggatggaaaa 120 acgtttgcag tcttttttgg ttggcatgaa acactgactg cattcctccc agatttataa 180 gaaagaaata tttgcagtct tacctggagt tagatggatg gactctctca aggttatttt 240 tcaatctctg cacatacata cttatggaag taagaaagaa gagggagaaa aggcagatcc 300 cccataacag cggttaaaca cctgaacttg ctccactatg acagggttta tcatccacct 360 ctcagtcctc aagtggctgg aaatatggaa attggagtcc aggtagacag gtgagtgtac 420 aacctcttaa gtgtggagcc ctcggaattc acaacactcc ccaaatcgct tcctgcgcag 480 gcgcggagtc ggaagggagt cggaaagcag accccggtgc cccctaataa agcccccagc 540 cggacgctgc cgctaccggg gtttggcaac ttccggaaga cctgtggccc aaaggagaat 600 cctgttgggg gaggcggggg ccggtggtcg ctaaccaatc cgacacccgc cagcaggctg 660 aagagagggg ctttcccaaa aggaaaactt tcccaaacct gggggatggg aagagaagac 720 aaaaggagcg cctctggctc cctttcccac ttcccagccg cccgtcccag ccctcggcct 780 ccgctgcgcg acccgggcgg aggatcccgg ccgcaggccg aggcgagagc caggcgggag 840 ggccgcgagc gggctgcccc tctccccgcc ttgccgtccg ccgctgacgt aacctgcgaa 900 gtttggggag ggaggagctc gggcggccgg agctggtcgc tgcgcgcgcc ggggggaggg 960 ccggggctgc gagagaggaa gctctttcgc ggcgctaccg cgttggcacc agtctctaga 1020 aaagaagtca gctctggttc ggagaagcag cggctggcgt gggccatccg gggaatgggc 1080 gccctcgtga cctagtgttg 1100 // ID HSA_8809_IL18R1 standard; DNA; HUM; 1100 BP. XX AC 8809; XX DT 05-Sep-2005 (Created) XX DE IL18R1: interleukin 18 receptor 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 102436627..102437726 (FORWARD) CC Score Points: 2 (66.7%) CC Chromosomal Location: 2q12 XX CC Database Reference HGNC: 5988; IL18R1 CC Database Reference ENTREZGENE: 8809 CC Database Reference UNIGENE: Hs.469521 CC Database Reference ENSEMBL: ENSG00000115604 CC Database Reference REFSEQ: NM_003855 CC Database Reference REFSEQ: NP_003846 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36377_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206618_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206618_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206618_at CC Database Reference TRANSFAC GENE: G003197; IL18R1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="2" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 102436627..102437726" FT /note="Genomic Strand: FORWARD" FT prim_transcript 989..>989 FT /db_xref="ENSEMBL:ENST00000233957" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [16182]; Alignment" FT prim_transcript 1013..>1013 FT /db_xref="ENSEMBL:ENST00000334376" FT misc_feature 1013 FT /note="SECONDARY ANCHOR: MMU [16182]; Alignment" XX SQ Sequence 1100 BP; 328 A; 203 C; 235 G; 334 T; 0 other; cagcttgtca ggactcaaac tggagtggca gcccaggttt gtgtgtttct gaaaccagac 60 tctgccatca ggctgtgctc cctgcactca ggatggtaaa caagggatat ggtgttgttt 120 atgcagtatt tagactctga atggtctcca ctgtggggga tccttcctcc actgggctca 180 aagttgtaat cagaactccg aatgctaggt tgcagtagga tcaaagttca atgcagatct 240 tagttccact gggacacagt caatgtaaag gaggggtctg gagtgtagga gactgtcact 300 tcatctctcc atttccctaa agtaaactca tatgggcagc cacagacaca cgcgaacaca 360 tgcatacaca cctatgcctc agtgacacat gttagtgagt gctggccatg tgctaggcat 420 cgtgctggat tttagtgata cagtgaagag caaaatagac ttagtgccta gaattatgaa 480 agaattatga aacctacgtt ctgaaggagg aagatggagt tttaaaaatt caaccctaaa 540 tgaagatctc attacaattc aggaatgttt tgatgtgaaa acacacacac acactctgtt 600 acatgggcag aactgccata catagctcag catgtcacag attgtttatt catagaatgg 660 taatatttgt agcagtacta ttgttctgaa ctttggcctt ggaagcagga tttagtagac 720 caggcctgaa attcttcaga ctctgttgta tcagagaaat aaattattag ggatttcttc 780 cagaagaaaa acttcattgc cttgaaattt tattaatttt atatggctga aagttctgag 840 aattggttac tatattaagg attataaaaa tcttctaggt tgttttttta aaaatctgtg 900 tgccagaaga tttttaaacc ttcataagat aggcacactt ttgtttgaaa gctttggctg 960 aatctgtttt attctgtttt ccagagaagc catttgaagc agaatccaaa ccatgaattg 1020 tagagaatta cccttgaccc tttgggtgct tatatctgta agcactgcag gtaagtgatt 1080 atacatactc tcaaacatat 1100 // ID HSA_8878_1_SQSTM1 standard; DNA; HUM; 1100 BP. XX AC 8878_1; XX DT 05-Sep-2005 (Created) XX DE SQSTM1: sequestosome 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 179179511..179180610 (FORWARD) CC Score Points: 127 (77.4%) CC Chromosomal Location: 5q35 XX CC Database Reference HGNC: 11280; SQSTM1 CC Database Reference ENTREZGENE: 8878 CC Database Reference UNIGENE: Hs.529892 CC Database Reference ENSEMBL: ENSG00000161011 CC Database Reference REFSEQ: NM_003900 CC Database Reference REFSEQ: NP_003891 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213112_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213112_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213112_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201471_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201471_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40898_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201471_s_at CC Database Reference TRANSFAC GENE: G003714; SQSTM1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 179179511..179180610" FT /note="Genomic Strand: FORWARD" FT prim_transcript 970..>970 FT /db_xref="dbTSS:CBR04531" FT prim_transcript 972..>972 FT /db_xref="dbTSS:HRC01732" FT /note="Number of reported TSSs: 2" FT prim_transcript 993..>993 FT /db_xref="ENSEMBL:ENST00000292588" FT prim_transcript 997..>997 FT /db_xref="dbTSS:LFL05193" FT /note="Number of reported TSSs: 2" FT prim_transcript 1000..>1000 FT /db_xref="dbTSS:MPG04457" FT /note="Number of reported TSSs: 6" FT prim_transcript 1001..>1001 FT /db_xref="EPD:EP73227" FT prim_transcript 1002..>1002 FT /db_xref="dbTSS:HRC04507" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:HUV00970" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:MPG04694" FT prim_transcript 1067..>1067 FT /db_xref="dbTSS:ColF5052.seq" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 192 A; 343 C; 369 G; 196 T; 0 other; tcccctggga ggtttctcca gctcctgcaa gccctgggct gaaatggcat gagttggacc 60 cagcaggttc tgacctccta ctcacaggac cttgcctggg aggctccaga gggtgaccac 120 tcgtcctgcc cctctccttg ccccagttct ggcggacagg ttactctggt ggcataaagc 180 agtgtttctt ccttcctagc tgaggaggct gttggctgac ccccttggct gcccacaagg 240 ccaacgggcc tgagccccca cagggccatg ggcattacct gctgaattga ggagcccata 300 aggagtcact tggaccacag tgaacacttg gcgaccactg acactcagga gaccttagct 360 ggtcctccag cacctctcaa ctccactcct actaaactgg gaacttctct ggtgctcagg 420 ccagagtcgg ggtccgtcac cgagtatgct atgcgctgcc catcaccgag gatgccatgc 480 gctgtaagag ggctgccacc gcggcaggct gaccatggca gggtcggaac agcaacctga 540 gagccagctt gttctggcca gcagtgccca ctgggcgacc tagcagcctc ctgatatggg 600 ggctgtgtcc ccctctccct gcactgggta cccccaactg aggatattgc tgagtcatgg 660 ccaggcccaa gcctgggagg ggcgaggggc tggacccccg ccagtaccct gatcccaggt 720 gcagaggctg gagcccaggc ctgtatgagt gccagggccg gtttcctggg gtccttggtg 780 caccggggca atgaagagag gggtcagcaa tgagggggcc gggagacctg gagcgagggg 840 tagcggggaa ggggagagta gtgaaggggc ctctgcaggg cggctctcgc gccgcgacga 900 cggtggcggg ggcggggagg gcgcgagaga ctccgcccct ctcgaggcgg ggcggggcct 960 ccgcgttcgc tacaaaagcc gcgcggcggc tgcgaccggg acggcccgtt ttccgccagc 1020 tcgccgctcg ctatggcgtc gctcaccgtg aaggcctacc ttctgggcaa ggaggacgcg 1080 gcgcgcgaga ttcgccgctt 1100 // ID HSA_9235_IL32 standard; DNA; HUM; 1100 BP. XX AC 9235; XX DT 07-Sep-2005 (Created) XX DE IL32: interleukin 32 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.16 3054631..3055730 (FORWARD) CC Score Points: 68 (100.0%) CC Chromosomal Location: 16p13.3 XX CC Database Reference HGNC: 16830; IL32 CC Database Reference ENTREZGENE: 9235 CC Database Reference UNIGENE: Hs.943 CC Database Reference ENSEMBL: ENSG00000008517 CC Database Reference REFSEQ: NM_004221 CC Database Reference REFSEQ: NM_001012718 CC Database Reference REFSEQ: NP_001012649 CC Database Reference REFSEQ: NM_001012635 CC Database Reference REFSEQ: NP_001012736 CC Database Reference REFSEQ: NP_001012650 CC Database Reference REFSEQ: NP_001012653 CC Database Reference REFSEQ: NM_001012632 CC Database Reference REFSEQ: NP_001012652 CC Database Reference REFSEQ: NM_001012633 CC Database Reference REFSEQ: NM_001012631 CC Database Reference REFSEQ: NP_001012654 CC Database Reference REFSEQ: NM_001012636 CC Database Reference REFSEQ: NP_004212 CC Database Reference REFSEQ: NM_001012634 CC Database Reference REFSEQ: NP_001012651 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203828_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203828_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203828_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="16" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 3054631..3055730" FT /note="Genomic Strand: FORWARD" FT prim_transcript 684..>684 FT /db_xref="ENSEMBL:ENST00000008180" FT /note="Number of reported TSSs: 2" FT prim_transcript 752..>752 FT /db_xref="dbTSS:CBL05763" FT prim_transcript 775..>775 FT /db_xref="dbTSS:STM07519" FT prim_transcript 789..>789 FT /db_xref="dbTSS:HbmA230057.seq" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:TMS09079" FT prim_transcript 1009..>1009 FT /db_xref="dbTSS:HRC07947" FT /note="Number of reported TSSs: 2" FT prim_transcript 1010..>1010 FT /db_xref="dbTSS:PCD00271" FT prim_transcript 1011..>1011 FT /db_xref="EPD:EP73018" FT prim_transcript 1012..>1012 FT /db_xref="dbTSS:REC00694" FT /note="Number of reported TSSs: 2" FT prim_transcript 1013..>1013 FT /db_xref="dbTSS:ColF5607.seq" FT prim_transcript 1015..>1015 FT /db_xref="dbTSS:PNC04873" FT prim_transcript 1019..>1019 FT /db_xref="dbTSS:FMR03147" XX SQ Sequence 1100 BP; 213 A; 351 C; 316 G; 220 T; 0 other; caggcagaac gtgatgaaga tgaagatggc catctacaag ggcaggagaa acctgaacag 60 aatcccagct ccgggccctc agaaggaccc cacgctgccc acattgacct tggacctcca 120 gcctgcagat cgtgagggaa gagacgtctt cgacttaggg ccccttgtcg tggtacttcc 180 ttagtttggc cccaggaaac catcccaaag gcaagggcgt ggttgtgctc agctggggga 240 agggggctgg gggccgtgag gaggaggtgg gaggcccagc caggctggag ggtcagaacc 300 cgtggagcta gaagagcccg taggggagcc ccaagattgc tgagaccagt gaccttcggc 360 cccagatggc cttgccttgg cccagaaggg tcagaaggac ctggtcagcc aagctcagac 420 agccggcagg atgccttcca ccctgcagag ggtcctatct tgtcccacag gtagatctac 480 atcaccacta gccacccctc caacgtgcac aggcccctgc cctcacggcg cccctcttag 540 gtccggcagt tcctgcctcc ttctgatcca gaagtttctc tggcctctgg agccggggca 600 cacctcatgc aaggacaggg tccaaattcc tttgtccttg gatcccactt ggctgacgtc 660 accttcctgt actcagggag tttccccagc cagctgtccc gagtctggac tttccctctg 720 cccctcccca ctctcaggct ggtggggtgg ggaaagcagc ccattcctgg gctcagagac 780 tcccacccca gctcagaggg agcaggggcc cagccaggga cggaccctca ttcctcccag 840 ggaccccaga cctctgtctc tctcgggtaa gtctccatct ctgtctgtct ctgtctctgt 900 ctctgtctct gtctgttttt cacgcactca gcaaggcctc ctgccctgag agaggctccg 960 cccactaccc cccactttcc ccataaaacc agctgagtat ttgtgccagg aagactgcgt 1020 gcagaaggtg actgtctcag tggagctggg tcatctcagg tggggagttg gggtccccga 1080 aggtgaggac cctctgggga 1100 // ID HSA_961_CD47 standard; DNA; HUM; 1100 BP. XX AC 961; XX DT 06-Sep-2005 (Created) XX DE CD47: CD47 antigen (Rh-related antigen, integrin-associated signal DE transducer) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.3 109292448..109293547 (REVERSE) CC Score Points: 23 (95.8%) CC Chromosomal Location: 3q13.1-q13.2 XX CC Database Reference HGNC: 1682; CD47 CC Database Reference ENTREZGENE: 961 CC Database Reference UNIGENE: Hs.446414 CC Database Reference ENSEMBL: ENSG00000196776 CC Database Reference REFSEQ: NM_198793 CC Database Reference REFSEQ: NP_001020250 CC Database Reference REFSEQ: NM_001777 CC Database Reference REFSEQ: NM_001025079 CC Database Reference REFSEQ: NP_001768 CC Database Reference REFSEQ: NM_001025080 CC Database Reference REFSEQ: NP_001020251 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213857_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:226016_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:61356_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:54922_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:227259_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211075_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213857_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:226016_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213055_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211075_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:227259_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211075_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213055_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213857_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213055_at CC Database Reference TRANSFAC GENE: G005895; CD47 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="3" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 109292448..109293547" FT /note="Genomic Strand: REVERSE" FT prim_transcript 953..>953 FT /db_xref="dbTSS:SPL09673" FT prim_transcript 964..>964 FT /db_xref="dbTSS:JTH09065" FT prim_transcript 966..>966 FT /db_xref="dbTSS:CNR04363" FT /note="Number of reported TSSs: 3" FT prim_transcript 978..>978 FT /db_xref="dbTSS:T3R02981" FT /note="Number of reported TSSs: 5" FT prim_transcript 980..>980 FT /db_xref="dbTSS:T7R03473" FT /note="Number of reported TSSs: 2" FT prim_transcript 982..>982 FT /db_xref="dbTSS:SZR07251" FT prim_transcript 992..>992 FT /db_xref="dbTSS:T3R00533" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [16423]; Alignment" FT prim_transcript 1003..>1003 FT /db_xref="dbTSS:T7R07857" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:FMR08563" FT prim_transcript 1008..>1008 FT /db_xref="dbTSS:COR05423" FT prim_transcript 1021..>1021 FT /db_xref="dbTSS:T3R00308" FT prim_transcript 1023..>1023 FT /db_xref="dbTSS:T3R07757" FT prim_transcript 1024..>1024 FT /db_xref="dbTSS:T3R06971" XX SQ Sequence 1100 BP; 207 A; 310 C; 439 G; 144 T; 0 other; gccttgtccc tattgtggct tgcggccaca tttcgaaccc atttttcaag catgttaaac 60 ccaagcgcag cgcagagggc tgcacatggg gcagtcacaa accaagctca ataaccttgc 120 tggtggggat gtgttggata cgctgctaat gcctgtttgc gacaatgctc gctagtcccg 180 gtggtggcgg tgttcacagg taacaatgtt taccaccgtg aatggaactt gtttgattaa 240 ccctgatcag aggatgaaaa cactaaagaa ccaagtgaga aagagggaag agaaccgcat 300 agggaagagc agagcgagta gacgagccga acgcagagcc cgcgaggggc gagtggaagc 360 tccctgcggg caggtacccg accaccgccc tgccctgggc gtggcggcct cgggctcagg 420 gaccgcttcg gcgctagacg gccgcgtccg gaggaaacgg gcgctggtga aagcctaggt 480 gtcctggtcc acgcgcgcag ccggacgtcg ggtccaggga gagacgcggg ctggggcggg 540 acgggacccg gcccctgaag cgcgagggtg ggagtgaaag caaagaggag aaaagtagag 600 agagaggaca gtggggccca gcgccgcgcg aaaggcagga accgacccgc ggacaggaac 660 gggtgcaatg aggtccccgg cgagcgtggg aacacagggt tcagcctcct gcggcgggcg 720 agcacgcgga ccccaggggc gggcgggtgc gacaggacgt gacctggaag cgcggcgcgt 780 gccaccgccc tggagcaggc atccggcctc cgtggagcgg gcaggcgggc cccgggtctg 840 gagcctgcga ctggggaggg cgccgcgtca acagcagcgg ttgcggggcg gggccgagtg 900 cgcgtgcgcg gctctcgcgg gcggggagca ggcgggggag cgggcgggaa gcagtgggag 960 cgcgcgtgcg cgcggccgtg cagcctgggc agtgggtcct gcctgtgacg cgcggcggcg 1020 gtcggtcctg cctgtaacgg cggcggcggc tgctgctccg gacacctgcg gcggcggcgg 1080 cgaccccgcg gcgggcgcgg 1100 // ID HSA_9619_ABCG1 standard; DNA; HUM; 1100 BP. XX AC 9619; XX DT 07-Sep-2005 (Created) XX DE ABCG1: ATP-binding cassette, sub-family G (WHITE), member 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.21 42508335..42509434 (FORWARD) CC Score Points: 1 (25.0%) CC Chromosomal Location: 21q22.3 XX CC Database Reference HGNC: 73; ABCG1 CC Database Reference ENTREZGENE: 9619 CC Database Reference UNIGENE: Hs.124649 CC Database Reference ENSEMBL: ENSG00000160179 CC Database Reference REFSEQ: NP_997510 CC Database Reference REFSEQ: NM_016818 CC Database Reference REFSEQ: NM_207628 CC Database Reference REFSEQ: NM_207174 CC Database Reference REFSEQ: NM_207629 CC Database Reference REFSEQ: NP_997512 CC Database Reference REFSEQ: NM_004915 CC Database Reference REFSEQ: NP_997513 CC Database Reference REFSEQ: NM_207630 CC Database Reference REFSEQ: NP_997057 CC Database Reference REFSEQ: NP_997511 CC Database Reference REFSEQ: NM_207627 CC Database Reference REFSEQ: NP_058198 CC Database Reference REFSEQ: NP_004906 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204567_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211113_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211113_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211113_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204567_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204567_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41362_at CC Database Reference TRANSFAC GENE: G009055; ABCG1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="21" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 42508335..42509434" FT /note="Genomic Strand: FORWARD" FT misc_feature 46..121 FT /note="ChIP-on-Chip Fragment: cMyc" FT /note="PubMed:14980218" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000347800" XX SQ Sequence 1100 BP; 271 A; 284 C; 283 G; 262 T; 0 other; ggggcaattc aagtcaccaa gccagtctca ccccaatggc ctggctggtt gcagaaactc 60 accagggaca aggggtcacc ccaccacagg cccacctgga catgtgactc ccctgcaccc 120 accctcacaa gcaccaaggg caggatcctc acgccagagg ccaagtcctc agtgtgcccc 180 tttctcccct tcatgttcag cctcagcagc tggaagtcca cagaaataaa tcagacactt 240 ctaaaatggg acaccatagg gaaggccaga tggaataaga gttctcttcc cacagaccta 300 gacttccatt gactccactc gaagtcaact gggtgatgct gttggctgca agtcaaggcc 360 aacatgggct gtgctaatag atgcagaccc tctagaggga aggagcacat caccctggcc 420 tgttctgtcc tgatcacact gaataggtgt tctttggtgg ccctgaattt catgagggac 480 acgaggaact ggcacccatc ccgagaaggg gaaagtggga caaaagggcg tcttctagga 540 agccacactg gagagactgg gggcatctgg tccagagaac aagggtctgg aaagaatgtt 600 gttgccatca ttggctggcc agggcctact ctggggagtg actccatgtt gctatggtgt 660 gcagagcagt cagggtgata gggagtccaa ttggacacag gttcagtttg ctaatggtga 720 caacacttaa taatggagtg ggttgccagt tgaggtagtg atatagtttg gctgtgtccc 780 cacccaaatc tcatcttgaa ttgtagctcc cataattccc acatgttgta ggaaggacct 840 ggtcagagat cactgaatca taggggcagg tctttcccat gctattctca tgatagtgaa 900 taagtctcat gagatctgat ggctttataa aggggagttt ccctgcacaa gctctctctc 960 ttgtctgccg ccatgtgaga catgcctttc accttccgcc atgatcatga ggcttcccca 1020 gccacatgga actgtgagtc cgttaaatct ctttcctttg taaattgccc agtctcaggt 1080 atgtctttat cggcagcgtg 1100 // ID HSA_9945_GFPT2 standard; DNA; HUM; 1100 BP. XX AC 9945; XX DT 06-Sep-2005 (Created) XX DE GFPT2: glutamine-fructose-6-phosphate transaminase 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.5 179712821..179713920 (REVERSE) CC Score Points: 4 (40.0%) CC Chromosomal Location: 5q34-q35 XX CC Database Reference HGNC: 4242; GFPT2 CC Database Reference ENTREZGENE: 9945 CC Database Reference UNIGENE: Hs.30332 CC Database Reference ENSEMBL: ENSG00000131459 CC Database Reference REFSEQ: NP_005101 CC Database Reference REFSEQ: NM_005110 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39640_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205100_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205100_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205100_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="5" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 179712821..179713920" FT /note="Genomic Strand: REVERSE" FT prim_transcript 979..>979 FT /db_xref="dbTSS:FBR01404" FT /note="Number of reported TSSs: 2" FT prim_transcript 990..>990 FT /db_xref="ENSEMBL:ENST00000253778" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [14584]; Alignment" FT prim_transcript 1057..>1057 FT /db_xref="dbTSS:KGR02266" XX SQ Sequence 1100 BP; 172 A; 377 C; 386 G; 165 T; 0 other; aggatttttt taagaaaaaa aaaaacttca aagtgcgcaa acgttgggcc ggttctcgtg 60 accttcctcg ggagacgagg ggcccagagt gcagggggaa cgggagggac ggccgggaac 120 cagggcggag aaacgcgggc cttggtgcct cactgggggg tcggattccg accccaggcg 180 taggaacccc cgggtccctc gcgggcctgc agcgcgaggc agatctgggg agggggcagc 240 tcggcgcggg tggggtcggg gcttcctggg gcgcctccag cttcgttcac aacctgcgga 300 accctcgcct tcaagctcgg gctccgcggc aaatcccagg gtcgaattct gccaccgccg 360 cggcgtccgg ttttggcaga gtccttgtct gcctccggga gcctcggttt tctcgtctct 420 ccgccaagcc cgggcgttct ctccacgcag ggtgagggcc aggcttagag gtctgcggag 480 ctctgaaaca agcctgtcac tcagatggga gcgcggcagg aacagcggct cacgcgggtt 540 tccggagcgc gcgagtgatg ccggacccct cgctctgccc cttacgcggc ccgtctgact 600 tctcagcacc ccgtgggagg gagcttccct gggtagcccc gtttcacaga cgggaaagcg 660 gaggcacagc gcgatcgggc cctgcccggc ttccacgcct actctggttg agtcggggtc 720 tgaactcggg ccgttggttg ccctaagccc cgctccggga tctggcgccc ggcgccccag 780 ccttacacgc ccgacccgcg cctgggagcc gcccctcggc ccccctccct ggctcctggg 840 ggccgggtcc cgtcgttgtc acgacaaccg ggggccaatg ggagcaggcg ggcgggggaa 900 gccccgcccc ttccccgccc ccttccccgc cctctcggag ggctccgggt tataagggct 960 ggaggccgag cggacgggag ctggagcccg cggagcccac ggagcccacg gagcccacgg 1020 aggagcccac ggaggagccc cagcgtccga acgggcagac cccctcgagc cgcgaaggag 1080 cccgagaagc agccacgatg 1100 //