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 Datab