ID HSA_10203_CALCRL standard; DNA; HUM; 1100 BP. XX AC 10203; XX DT 07-Sep-2005 (Created) XX DE CALCRL: calcitonin receptor-like XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.2 188138400..188139499 (REVERSE) CC Score Points: 3 (37.5%) CC Chromosomal Location: 2q32.1 XX CC Database Reference HGNC: 16709; CALCRL CC Database Reference ENTREZGENE: 10203 CC Database Reference UNIGENE: Hs.470882 CC Database Reference ENSEMBL: ENSG00000064989 CC Database Reference REFSEQ: NM_005795 CC Database Reference REFSEQ: NP_005786 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206331_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206331_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:59645_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210815_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:234996_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:234996_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210815_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210815_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206331_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:42475_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34995_at CC Database Reference TRANSFAC GENE: G007290; CALCRL 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: 188138400..188139499" FT /note="Genomic Strand: REVERSE" FT prim_transcript 994..>994 FT /db_xref="dbTSS:HCR07021" FT /note="Number of reported TSSs: 2" FT prim_transcript 1015..>1015 FT /db_xref="dbTSS:HCR03249" XX SQ Sequence 1100 BP; 380 A; 208 C; 155 G; 357 T; 0 other; aaaagcattt taaatttaca ttttcccctg atcatatcca atgatgtatt aaacatattc 60 aggaaaaact atgctttgag atgaaatttt gtctaagaaa taaagtatcc tttgtattta 120 tattatttta taatattatg tttacaacat ctatattttc tttaagatta tattgactta 180 caaatattgt ggtataaatt attttatatt ataaataaca taattatacc aaatattttt 240 aaatgtgtgc aataatttta aaattatgaa ttattcaaaa ggctattttg tcaaatatat 300 atacttatat attataaaag aaacactcta tacacacaca tacacaacct gaatttataa 360 cacatacact catgttctta tgaagaaggt aaaggaaaaa ataaaagatt taaaaactgc 420 aggataaagt ttcttgatct aattaactga ttaggaactg cacttaggaa ctgatggagg 480 aacagcaccc aattagcaga gctccaaatt aagaagagcc aaatcacaaa accagttatg 540 atgaatacag ttaatttttt tttctgtgtt gtgctatgaa cacagatttg ttagattttt 600 tttcctggat actttgtaag ctataattca acacacacac acacacacac acacacacac 660 acacacacac gcctaactcc tttgattctt tgagcagaat actatattca gatttccttc 720 aaatcacaag tagcttgttt ggcaagttct aacagaactc agtcaaggtg aaagccagcc 780 agctttttac tggtaacaat gtattcacac agcctatgat ctctctctgt tcaggctgct 840 tcttgctctt gtctcacaat aagaaaggag tgctgctttc ctggggtatg ctatttgaga 900 aagaaagtaa cctaacacta actgcaggcg gggtcagagt gatgtaacag gaagctctga 960 tgtttccctt ctgctgctga tcacttacaa tctgacaaca cttacaatct actcagaaca 1020 acctctctct ctccagcaga gagtgtcacc tcctgcttta ggaccatcaa gctctgctaa 1080 ctgaatctca tcctaattgc 1100 // ID HSA_10370_CITED2 standard; DNA; HUM; 1100 BP. XX AC 10370; XX DT 06-Sep-2005 (Created) XX DE CITED2: Cbp/p300-interacting transactivator, with Glu/Asp-rich DE carboxy-terminal domain, 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 139737351..139738450 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 6q23.3 XX CC Database Reference HGNC: 1987; CITED2 CC Database Reference ENTREZGENE: 10370 CC Database Reference UNIGENE: Hs.82071 CC Database Reference ENSEMBL: ENSG00000164442 CC Database Reference REFSEQ: NP_006070 CC Database Reference REFSEQ: NM_006079 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:207980_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:207980_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209357_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:33113_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:207980_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209357_at CC Database Reference TRANSFAC GENE: G005400; Cited2 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: 139737351..139738450" FT /note="Genomic Strand: REVERSE" FT misc_feature 390..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000306105" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [17684]; Alignment" FT /note="PRIMARY ANCHOR: RNO [114490]; Alignment" XX SQ Sequence 1100 BP; 225 A; 325 C; 376 G; 174 T; 0 other; caagtttgta cacaccccca cctcccggat ccagggcaac agcagaagca agtaactgtg 60 tatgtgcaaa aaggtggatc tggggacgag gatcgctgag tttgtttaca gagcagagac 120 gcctcagctc ggatgccaaa gctaccaaga gctgcaaacg caaacttagc agaagcacac 180 gtaccccggg agcggcaggc gggcccgaaa gcgcggactg gaattccagg gcgcgggagc 240 gggggtggcc gggccctcga gcgcgctccg tccacctgca gcggctgccc ctccccgccc 300 ccagctcctg tccttgaaag gagtggagga aaaaaatgca tctacaagcg gtgatctaga 360 gtaggtctac ccactgcccg tatgaaaaca caaaggcaca gcctaggaag gcgcgctcag 420 gaaagggcgc attatttgtc cgggtcttta aaacccaact cgaggaagca cagccattct 480 tcgctgcctg tggaagcttt tgcaaaaccg gggaggcaca agggcactct ggagggcggg 540 gggcgctggg cgagtcccct tttcccgtag agagcggggc agatcgctag gtgaaccgag 600 tgagaaagct gggggtgggg tagatccagc ctgagggggg cggtgagctc tcctcgtggc 660 tatcccggca ggctctacct tcgggcgggg cggcagggga ggattttccc cctgcctcgg 720 gggtggctga gccaacctcg cgtttctggg ccgggaagaa accagagtcg gggggcgacg 780 gggcgactgg gcggcccccg ggccccgcag cctctgcagc acgtgccgcg ggcggcgggg 840 acgcggctcc gggacccggt ccagggtgtt cgcggtgttc cggaatccgc gtcttggcgc 900 cgcccgccct ggaggctctc gctccgcctt tccgaaatgc ctatattaac tgtggccaaa 960 gccctaagaa acacagctca ttgttggcag ctgccgggcg gtcctgccga gctgtgaggg 1020 caacggaggg gaaataaaag ggaacggctc cgaatctgcc ccagcggccg ctgcgagacc 1080 tcggcgccga catcgcgaca 1100 // ID HSA_11080_DNAJB4 standard; DNA; HUM; 1100 BP. XX AC 11080; XX DT 06-Sep-2005 (Created) XX DE DNAJB4: DnaJ (Hsp40) homolog, subfamily B, member 4 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 78155927..78157026 (FORWARD) CC Score Points: 3 (17.6%) CC Chromosomal Location: 1p31.1 XX CC Database Reference HGNC: 14886; DNAJB4 CC Database Reference ENTREZGENE: 11080 CC Database Reference UNIGENE: Hs.380282 CC Database Reference ENSEMBL: ENSG00000162616 CC Database Reference REFSEQ: NP_008965 CC Database Reference REFSEQ: NM_007034 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203811_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203811_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203811_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203810_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203810_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:158_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:62561_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203810_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: 78155927..78157026" FT /note="Genomic Strand: FORWARD" FT misc_feature 355..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT misc_feature 679..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT misc_feature 868 FT /note="PRIMARY ANCHOR: MMU [51886]; Alignment" FT prim_transcript 977..>977 FT /db_xref="dbTSS:HRT07430" FT prim_transcript 982..>982 FT /db_xref="dbTSS:HPR09406" FT prim_transcript 1045..>1045 FT /db_xref="dbTSS:LNF05537" XX SQ Sequence 1100 BP; 280 A; 274 C; 289 G; 257 T; 0 other; tacaaagagg tctggtcagt ttacgactct gaactgagag gcagattcaa attgaaacct 60 ctggtataat gggcctgagg ccattttgag aaataagggg ggcggactgg tggaacagac 120 tgacacgtaa atcccgccca gaaaaaggct gctttcaagt cccttccttg tagaggtgtg 180 acggtgaatg gtactgaaag cggttttaat tgcgagagag aacggaaatg agctgtaaag 240 gctactttaa tgataaatcc cttcccttgc tatggctcca ggacagaccc tagttctttc 300 ccaaactcat taccagaacc ttccattaaa ttgtgtgaaa ctaactgcgc tttatcccct 360 ggaagaggat ctttatctaa actagctcac tggagacacg cgagtgccgc agaagcggga 420 gaaagacttc aggccttctt tgcgtagcac gcgtcggggt tctaagtgga ttaggcacca 480 agaacacaaa actgggttct ggtctctaat cgttattacc aacatgggga aacgtgtctc 540 ttcacatttc agcccggaag aacacctctt tcctcttcct catgcgctta agggtagcgg 600 cctactcagt cagcggccaa ttaccgtgag ctttcgggat tccgccgcgc ggtccacact 660 tacctgccgg gctctctgca gtgcatcttt gaaagcgtcg ttaactcctc caccaccacc 720 gccgccacca ccgccaccag ctgagccaga agagggggga ggcactgttg aatagtctgc 780 catggttgca ctataagagc cgctgccgcc tgttcagaga cttcctctca gctaacagct 840 aagaaagaaa gaaaatggcg gccgtcgaag ctctattaca ttcttgcgcg accatcgtgc 900 cgtaaagggg cggagactga aggaacaaaa tctcgcgatg tttccgaggc aacgcgctgg 960 tgtgggttag ggctgagaaa gaacgacagg aacagagacg tcgcgaggat taagtttaag 1020 acttcgcgag aacagaattt cttttggcac ctcctctccg cgcgttcttg gggtgaggct 1080 gggtaattgt tcctgcaggg 1100 // ID HSA_115207_KCTD12 standard; DNA; HUM; 1100 BP. XX AC 115207; XX DT 05-Sep-2005 (Created) XX DE KCTD12: potassium channel tetramerisation domain containing 12 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.13 76358442..76359541 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 13q22.3 XX CC Database Reference HGNC: 14678; KCTD12 CC Database Reference ENTREZGENE: 115207 CC Database Reference UNIGENE: Hs.109438 CC Database Reference ENSEMBL: ENSG00000178695 CC Database Reference REFSEQ: NP_612453 CC Database Reference REFSEQ: NM_138444 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212188_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212192_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:212188_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212192_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:64269_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38972_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:49298_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:212188_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:212192_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="13" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 76358442..76359541" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000317765" XX SQ Sequence 1100 BP; 215 A; 313 C; 364 G; 208 T; 0 other; gatatataaa tatccctttc tgagactgac gggaacttgg acagggccga agagtgaccg 60 aggcatgcgg gagagaaggg gcgcctggac ttttggaagg ataaacatgc aggcgccaaa 120 ggtggcttta aaaattacgt tagatctgca actgttgtga gtctaagggc gcgattcaac 180 gaaggctgaa tgggacccgg agaccgaacg ttccggagtc ttaccccttc acttcgaagt 240 gaagtgcctc gaaggccctg cgggaagagg gaattgcaat taagagcaga tttgaagctt 300 catctcattt tgtctctgca gccagaaaat aaactatcgt aaagcatcct actgcgggac 360 actgaggttt gctttttgtt tctaggttta tttatttatt ttccaggctg gctgcaaggc 420 aacttgaaca aaatctggct gcgctcggac tggggcggct ctttcgtctc tccaggtttt 480 tcgcgtctct ctactttcag tgacacgaca accaacgatg gcaggccgca gctgcactgc 540 tggaagcgcc cagttccgca ggcgggaggg ccggaggcgg ccacgcattt ccactcccgg 600 ggcgacaggc ttccgaaagt tcacgtcctc cttccagagt ccttgggtgc gggctggggc 660 gagaggggag ggggcgcggt gactgtccct ccaaggagct gtcttccgaa gccgccaagt 720 ctcgggcggg tcctcttcgg aagagggaga aagttgggcg ggaccacggg gcggggctgg 780 tgggtgggga gcgggtggga gtccgggcgc ccccagcgct cgcgagccgg ggtggagcca 840 gcagccccgc gtggcgtccg cgtttaagat gcaaatcgag tccccgctcc ccacctcccc 900 tcgcccggta agcgaggctc cgccgccgcc cacgcctcct gcgcgccacg gcaccagagc 960 aggcggctct acttaagcag cgcgcgggcc gcgacccggc actcgcctgg agcgcgcggg 1020 caaggcgggc ggagcgcact ggaactcaag ggggcgcaca gcggcgcgct cgcaccgctc 1080 ggctccgcgc ggctctagga 1100 // ID HSA_1602_DACH1 standard; DNA; HUM; 1100 BP. XX AC 1602; XX DT 06-Sep-2005 (Created) XX DE DACH1: dachshund homolog 1 (Drosophila) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.13 71339198..71340297 (REVERSE) CC Score Points: 4 (100.0%) CC Chromosomal Location: 13q22 XX CC Database Reference HGNC: 2663; DACH1 CC Database Reference ENTREZGENE: 1602 CC Database Reference UNIGENE: Hs.129452 CC Database Reference ENSEMBL: ENSG00000165659 CC Database Reference REFSEQ: NP_542937 CC Database Reference REFSEQ: NM_004392 CC Database Reference REFSEQ: NP_542938 CC Database Reference REFSEQ: NP_004383 CC Database Reference REFSEQ: NM_080759 CC Database Reference REFSEQ: NM_080760 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205471_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205471_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205471_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="13" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 71339198..71340297" FT /note="Genomic Strand: REVERSE" FT prim_transcript 967..>967 FT /db_xref="ENSEMBL:ENST00000305425" FT /note="Number of reported TSSs: 3" XX SQ Sequence 1100 BP; 267 A; 286 C; 212 G; 335 T; 0 other; tttgggtctt aaaggacatg aggatagttg gttactgtgt aagacaggtg aattaattat 60 agagttttgg gtaagaaaac cctttttcca ctttctaaat cttcaaggat accttatctc 120 cttgatagct ctaggtttaa caggtatttc tgactggctt ttggggagac agtgaagtta 180 ttctaaatca tccacatcaa ggcaagcatt tctttccaca acctattagg aaatatggaa 240 ttgaatacag agctttccat tattcttaag cgatttcgga ctgactttct tctcaccact 300 tgaaaactgt cctggaattt tcactatctt tatataaata aataatttag tagagaaata 360 aacaatcaga tgcaaaagaa cattacgctt tgcttacatg tgaattttcc tcaaaataat 420 ttctgaataa tcgtgaagtg ggggctgtgt tttcgtttct agctcattgc caaaacgcgt 480 ggagatggat cctaaatcct ggaaggagag agctcggcgc gctcaggctc ctctttaagt 540 tggcgggcga ttgtttagaa gctttggaaa aaattaccag tccccgcgga cgaaatggaa 600 tgtgagacat gcaatctaac ggtagtagta gaagagaagt agatgatctc cctctccttt 660 tccgatcgcc acttctgtgt ccccggcttt tcctctccgt ccctcccaca gtttctttcc 720 gtatcctccc cctcccctcc tcctttcctc gcacgctccc tctccagtgt ctcgcgctct 780 cggagtctct gctccgagtt cctggttgga taatttgggt taatactagt gagtgaggtt 840 tttgcggctt caaagggtat ttcaagtttc cggagctcct cccctctgca ccgtgtgaca 900 acaacaactc gtccagccgg cagcctgcac ttttcagctc attttctctc tgtcattccc 960 ctctcaatct ttgatcaatg tacttgccag ggagagccca agtccttcaa acctcctcct 1020 tttcaccttc atccttaact ttgtgctaga gcgagaccca cacaacaaca gccgaccctc 1080 cccgccccac ccccaccccc 1100 // ID HSA_1846_DUSP4 standard; DNA; HUM; 1100 BP. XX AC 1846; XX DT 07-Sep-2005 (Created) XX DE DUSP4: dual specificity phosphatase 4 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 29264004..29265103 (REVERSE) CC Score Points: 20 (95.2%) CC Chromosomal Location: 8p12-p11 XX CC Database Reference HGNC: 3070; DUSP4 CC Database Reference ENTREZGENE: 1846 CC Database Reference UNIGENE: Hs.417962 CC Database Reference ENSEMBL: ENSG00000120875 CC Database Reference REFSEQ: NM_001394 CC Database Reference REFSEQ: NP_476499 CC Database Reference REFSEQ: NP_001385 CC Database Reference REFSEQ: NM_057158 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204015_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204014_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204014_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1788_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:204015_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:204015_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:204014_at CC Database Reference TRANSFAC GENE: G004860; DUSP4 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 29264004..29265103" FT /note="Genomic Strand: REVERSE" FT prim_transcript 915..>915 FT /db_xref="dbTSS:AMR03180" FT prim_transcript 953..>953 FT /db_xref="dbTSS:KGR05051" FT /note="Number of reported TSSs: 4" FT prim_transcript 956..>956 FT /db_xref="dbTSS:T7R00252" FT /note="Number of reported TSSs: 2" FT prim_transcript 981..>981 FT /db_xref="dbTSS:JTH05624" FT prim_transcript 984..>984 FT /db_xref="dbTSS:KGR04646" FT /note="Number of reported TSSs: 3" FT prim_transcript 995..>995 FT /db_xref="dbTSS:ADG01734" FT /note="Number of reported TSSs: 5" FT prim_transcript 1000..>1000 FT /db_xref="ENSEMBL:ENST00000240100" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [319520]; Alignment" XX SQ Sequence 1100 BP; 204 A; 323 C; 395 G; 178 T; 0 other; tttttccccc gaccagggtt aaataaacat cttttaggaa gcgtggacag gagcgcagcc 60 tgctctcctc cctcggaaca ccattccggc aattaatgcc tccctttggg tagtaaagca 120 acaaacccca cacctcactc cgatcctggg cttcgggcgg gaggactttc tctttcatct 180 tccaagcagg gggttgccca cgttcttggg gaagctataa aactgattta atggctttag 240 atgaaaatcg atcacgctaa tgcatacgct aacgtctcag gaatcgcata ttcagaaagg 300 actggccggg ccgaaagcgc acggggagtc tggggctagg aggtgtcagg ccccgctggg 360 tgggcagcag cgctccggtc ccctctccac ttgggtaacc gggaaaaacc tacggggctg 420 tcacgcgggg aagcgcgaag gtgccaaggg atgaaagctc aaacccgagc cctggcctcc 480 tcagccggct atttcctttg gcgccgcccg cctagcggcg gggtgcagcg gcggcacagg 540 tgccggtgtc gggctggagg cgcggcgcag gctgggcccg cgggtagacg gcgaaaggcg 600 ccgcgcgctc cattcacaaa gtccgggcgc tgcccgccgc tggcggcggg tcggaggccg 660 cctccctctt cctctcggcc tcggttttat gaatgggcct gatggcgagc acccggcgcc 720 ctgtttactc cgctctttgt gacgtcgagt tcccgtgacc gggagccagc ggccgcgctc 780 cattcaagct ccggggaggg ggtgggagga ggggcccgga gggggcgggg agtcagcgcg 840 gggggcgggg gacagcgcgg ggggcggggg acggcgcggg gcccggaatg gaacggggcg 900 gggcctggcg gggtagtacc tagcgccccc tcccccggga gcgcggagga gcattaataa 960 acctctaagc cgaggagaaa actctggctg gggcagtgcg ctgagcgccg gaggagcgta 1020 ggcagggcag cgctggcgcc agtggcgaca ggagccgcgc gaccggcaaa aatacacggg 1080 aggccgtcgc cgaaaagagt 1100 // ID HSA_2012_1_EMP1 standard; DNA; HUM; 1100 BP. XX AC 2012_1; XX DT 06-Sep-2005 (Created) XX DE EMP1: epithelial membrane protein 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.12 13239973..13241072 (FORWARD) CC Score Points: 83 (82.2%) CC Chromosomal Location: 12p12.3 XX CC Database Reference HGNC: 3333; EMP1 CC Database Reference ENTREZGENE: 2012 CC Database Reference UNIGENE: Hs.436298 CC Database Reference ENSEMBL: ENSG00000134531 CC Database Reference REFSEQ: NP_001414 CC Database Reference REFSEQ: NM_001423 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201324_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213895_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:234233_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1321_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:37762_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201325_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:201324_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:201325_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:56675_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201325_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:234233_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213895_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:201324_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="12" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 13239973..13241072" FT /note="Genomic Strand: FORWARD" FT misc_feature 932 FT /note="SECONDARY ANCHOR: MMU [13730]; Alignment" FT prim_transcript 945..>945 FT /db_xref="ENSEMBL:ENST00000256951" FT prim_transcript 951..>951 FT /db_xref="dbTSS:COR01841" FT prim_transcript 952..>952 FT /db_xref="dbTSS:LNG13911" FT /note="Number of reported TSSs: 4" FT prim_transcript 954..>954 FT /db_xref="dbTSS:HCR04149" FT /note="Number of reported TSSs: 2" FT prim_transcript 955..>955 FT /db_xref="dbTSS:HCR02518" FT /note="Number of reported TSSs: 9" FT prim_transcript 969..>969 FT /db_xref="dbTSS:HCR07041" FT prim_transcript 972..>972 FT /db_xref="dbTSS:LNG05717" FT misc_feature 995 FT /note="SECONDARY ANCHOR: RNO [25314]; Alignment" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [13730]; Alignment" FT /note="PRIMARY ANCHOR: RNO [25314]; Alignment" FT prim_transcript 1014..>1014 FT /db_xref="dbTSS:HCR08878" FT /note="Number of reported TSSs: 2" FT prim_transcript 1015..>1015 FT /db_xref="dbTSS:SYN06353" FT /note="Number of reported TSSs: 61" FT prim_transcript 1021..>1021 FT /db_xref="dbTSS:COL03049" XX SQ Sequence 1100 BP; 284 A; 267 C; 279 G; 270 T; 0 other; tgcatgagaa aataggcatg gagaagttaa gtggtttgcc taaagtcaca cagcaaattt 60 gtggagagct gggcttgaac tcaggcatct gggcttttac tctctccagt ggaatgcctg 120 ggctgtggga tgagatgact tcacaggcct ctcccagctc cagagttgag agagagagag 180 gagtggtgca gggaggtagt agggatgatt atgctactgg ccaagttcaa gaaagtcaat 240 tgtagaacaa ggtccagctg attattacag agagcaaagt tcttaactag aggacttcct 300 cctggaatgt ggagagtcca cacgggcact agcagagcat aatgaaagac caggaattct 360 ctgctgttca atcagtgctc catcactcag aggcagggct gcaagagctc ctagtgtgtc 420 cccttcgcct tcagggcctc cctgtacagc cacccacagg acagtgcacc agggtcaggc 480 agggaagtaa ataaaaaaag gaatctgata attcctgaca gtgagcagca gctgatgctt 540 ttaatggggg aggaagactg ggaatctcgc ttgatgatga cctaggactt cagtcagcag 600 gacactggcc cctttcctcc ccctcccagg ctgaaacctt gtgttttgcc ttatgtccat 660 ggtaaccaag tctccttttt ggtgaggagg aatgggcttc agtaaacaga tctatttgtg 720 tgatcctgtt actcatttga agcaatgtcc ctcctttttt ccactgtggt ctgtgtgtct 780 gagtcagaga gagcctacaa cagggttctt tgaattgatg gctcactccc agccactctt 840 gactgactgc cagcttagca gggcgtagct taccaacaaa tctttttttt ttttttaaag 900 ccagactgat tcatagaaac tcctttaaaa cacggtgaaa agaaaccgcc cattacacac 960 cccagtacac cagcagagga aacttataac ctcgggaggc aggtccttcc cctcagtgcg 1020 gtcacatact tccagaagag cggaccaggg ctgctgccag cacctgccac tcagagcgcc 1080 tctgtcgctg ggacccttca 1100 // ID HSA_23255_KIAA0802 standard; DNA; HUM; 1100 BP. XX AC 23255; XX DT 07-Sep-2005 (Created) XX DE KIAA0802: KIAA0802 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.18 8706369..8707468 (FORWARD) CC Score Points: 2 (66.7%) CC Chromosomal Location: 18p11.22 XX CC Database Reference HGNC: 29121; KIAA0802 CC Database Reference ENTREZGENE: 23255 CC Database Reference UNIGENE: Hs.464563 CC Database Reference ENSEMBL: ENSG00000168502 CC Database Reference REFSEQ: NP_056025 CC Database Reference REFSEQ: NM_015210 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213358_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213358_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39614_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213358_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="18" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 8706369..8707468" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000306329" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 291 A; 194 C; 278 G; 337 T; 0 other; ggattggggg atgagttgcc atatctgtgc cctttccagt agaccattgt gtgcaggtaa 60 ggttgaccga agcatcatca tcaccccatt ttgtgccaac ccttattttt ccataaggat 120 tcacattttt atttgttgtg tttcttgtac ttaatcttac ctaggataaa cacatcttca 180 ggagatttct ttttgttcat tttttttttt tttttttttt gtctgaggct cggatgttgg 240 gcaccttgtt ctttattgtt agtcaattcc tgtttttaag aataaataca ggattagcat 300 gagtggtaaa aatccaggaa caaagggaat agcaggacga gaatggacaa ttagggtgtc 360 tgagtatagg agagattttt ttttcttgaa ccttaatatt aattgaataa agtaaatggg 420 aataactgag tgcatgctat tctggaggca tctgaaacta tcaattatga aactagtcaa 480 gaaaatccct agaatgtttc cttaatcttc ctccttccaa attgttcctc ctttaaatct 540 tgtgtaaccc ttcagtagag tgaatatctc atacctgcag ctacatctgt gggtttggga 600 agaagctttc atcactgggc tgcaagactg gaacaaagcg agcgtgcagt tgtgtctgat 660 gttagtcgcc tttctgactt ggtgtttgta agtgttcact ggcgcacctg tgtattcatt 720 cagcaatatt tattgaggac ctaccgtgtg ctccatgctg ctcgggatgc agagaggaga 780 aagacagaca agcttgctcc cctctgaagc ttaccttgtt agtgtaggtg acagacagta 840 agtaggaaaa aataccaata ctattagatg gcactcagag gtgggaagaa aatagagcca 900 gcaagagact agagactcgg gctgatgagg gtggccaggg gaggctttgc atgacgtcag 960 attatgtgat ggaatgagct ctgcagagat ctggagcggg gagtgttttc agaagtggga 1020 atagcaggcg aggtcttgag gcctgaagaa gcaaaggtgc gagcagtctc agaccctgtg 1080 ctagtcgtgg gcagggaggg 1100 // ID HSA_23554_TSPAN12 standard; DNA; HUM; 1100 BP. XX AC 23554; XX DT 07-Sep-2005 (Created) XX DE TSPAN12: tetraspanin 12 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.7 120091948..120093047 (REVERSE) CC Score Points: 2 (20.0%) CC Chromosomal Location: 7q31.31 XX CC Database Reference HGNC: 21641; TSPAN12 CC Database Reference ENTREZGENE: 23554 CC Database Reference UNIGENE: Hs.16529 CC Database Reference ENSEMBL: ENSG00000106025 CC Database Reference REFSEQ: NP_036470 CC Database Reference REFSEQ: NM_012338 CC Database Reference AFFYMETRIX: AFFY_HG_U133B:230625_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:230625_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:60041_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219274_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219274_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:57669_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="7" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 120091948..120093047" FT /note="Genomic Strand: REVERSE" FT misc_feature 524..>1100 FT /note="ChIP-on-Chip Fragment: HNF1a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT prim_transcript 920..>920 FT /db_xref="ENSEMBL:ENST00000222747" FT prim_transcript 1083..>1083 FT /db_xref="dbTSS:KDN00119" XX SQ Sequence 1100 BP; 307 A; 242 C; 251 G; 300 T; 0 other; tttttctgca aggaaatcca aggactccag ttattaggtc aaagatgttg ctcgtattcc 60 aggtaattca tatttgctgg tgaagtttta tttgccatgc agtgcccaca aaagtaatcc 120 tagaaatgag cagtactgtg aggcatagca caacacatcc acattttatg tggaggatat 180 gatccagtgg cattttattt agtgtgaaac ttctgtcttc taaaagggaa gattcttttg 240 gaaggatggt ctcctgctgt gtaatacttc atgaatttct agtttaaaaa aattagattt 300 tccaaagatc cactactatg tacacatttc aaaataaatc acccagttaa ctcaaaacaa 360 tcttatcgtg agaaattttg gaaagcttga gttacttcta agagttaaaa atgttctttc 420 ctcctcttct gcatgtcaga ctgcacatga ttactctgat gtttccgtaa atgctattag 480 tgcactatga aagtgggaaa gaacttaaaa aaaaaaaaat ccgggagggc aacaaagcaa 540 taagaaggat catagggcac catgttaata acaaatcaca ggaggtggct ccataaaggt 600 tgtgaaaact agtttctcat tgcaggaatt gggttgggcc accccttcac cccccttctc 660 aaacacaaat attatcatat aataaaagcc tgcttctcta tgcttataac ccagcctcca 720 ttccttcgac gccaccattt taaagggatt tactgcacgg acttctccca agttcctagg 780 cattatcttc tggaccctat cctgcagagg tgaagcgtcc ctttggggac tctcgctggg 840 tgagagggac aagaaacacc cactaggacc caaccccggc agccagcggc tcgagcatgc 900 gctgagagtt tgtgcagctg gccctggctg ccgccgctgc ctcgtccgga ctcggagagg 960 acttgggagg gacagcggcg ctgggaggtg gcttagcaga gactttccag caactgctgc 1020 ccaggacttt tttttttttt tttctttttc ccaggaggcg gcgacggcgg cggcgggggg 1080 agaggaagag aaagaagcgt 1100 // ID HSA_25945_PVRL3 standard; DNA; HUM; 1100 BP. XX AC 25945; XX DT 07-Sep-2005 (Created) XX DE PVRL3: poliovirus receptor-related 3 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.3 112272618..112273717 (FORWARD) CC Score Points: 3 (37.5%) CC Chromosomal Location: 3q13 XX CC Database Reference HGNC: 17664; PVRL3 CC Database Reference ENTREZGENE: 25945 CC Database Reference UNIGENE: Hs.293917 CC Database Reference ENSEMBL: ENSG00000177707 CC Database Reference REFSEQ: NP_056295 CC Database Reference REFSEQ: NM_015480 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213325_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213325_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:86478_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:34202_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213325_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="3" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 112272618..112273717" FT /note="Genomic Strand: FORWARD" FT misc_feature 921 FT /note="SECONDARY ANCHOR: MMU [58998]; Alignment" FT prim_transcript 938..>938 FT /db_xref="ENSEMBL:ENST00000319792" FT prim_transcript 980..>980 FT /db_xref="dbTSS:KGR08133" FT prim_transcript 1088..>1088 FT /db_xref="ENSEMBL:ENST00000319814" XX SQ Sequence 1100 BP; 177 A; 329 C; 421 G; 173 T; 0 other; gggaataagt gggctgggaa gaagggaagg attcggagag cacagctgtc ccggggaaca 60 ggaaggagga gaaagtctct ccctcccttc agtgccccgc gccccagcga ggaggaagat 120 tactagtcca gcaggctgcg tccagcttcc tacacaggaa cctttagcat gggcaacgga 180 agggcagccc cctcctgcct tcccctcccc accccacccc ctcgtcccag gtccccgcca 240 cagggagagc gccgcccggg agaggagaag gccgagcgtg attgtcccgc agccctcgcc 300 tcagtcggcg ccggggcccc cgtggacccg cgaggggtgg agtgggcgag accattggaa 360 aggcagggaa ggggggaaac caggcaggaa cgaggggcgg ggccgactaa cctattccag 420 attttcctgt cccttttaaa tctctgctgt gggagaaacc ccgttatcaa agtggatgaa 480 aagaatattt ttttttgaaa ggggaggagc atgtgtagga gggcggggtg ggaggagaca 540 gggcttgcgc ccggggatca gacgggaggt ggagttgcgc ggggagggcg ggcgagtcgg 600 gcgcccgctc tgagagtcgg tttcttttcc ccctcttgcg tggggcgggg tggtgcgttc 660 cgagttccca ggagttcgac gcgggcgggt gccgagggga ggggagtggc ggcggcggcg 720 ggcggctccc gcttcagcct cggcagtggc gtcggcgacg gcggtgtcga ggcagccgcc 780 agcgttcggc caagtgtcag ccggcagcga cggcgctaga gctgggagct ggggacgcgc 840 gcgccggacc ttccacagcc tccgcccaga gcctgaggcg ccggggccgg gggagccggg 900 gggcgggcgg gcgagcgggc cggggggagg gtgggggatg gcgcggaccc tgcggccgtc 960 cccgctgtgt cctggaggcg gcaaagcaca actttcctcc gcttctctcc tcggagccgg 1020 gctcctgctg cagcccccga cgccacctcc gctgctgctg ctgctcttcc cgctgctgct 1080 cttctccagg ctctgtggta 1100 // ID HSA_29775_CARD10 standard; DNA; HUM; 1100 BP. XX AC 29775; XX DT 07-Sep-2005 (Created) XX DE CARD10: caspase recruitment domain family, member 10 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.22 36239648..36240747 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 22q13.1 XX CC Database Reference HGNC: 16422; CARD10 CC Database Reference ENTREZGENE: 29775 CC Database Reference UNIGENE: Hs.57973 CC Database Reference ENSEMBL: ENSG00000100065 CC Database Reference REFSEQ: NM_014550 CC Database Reference REFSEQ: NP_055365 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210025_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210026_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210025_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210026_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41817_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210026_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210025_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41816_at CC Database Reference TRANSFAC GENE: G003618; CARD10 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: 36239648..36240747" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000251973" XX SQ Sequence 1100 BP; 158 A; 359 C; 444 G; 139 T; 0 other; tcacacctct ttcctgtacc ggttgtgcct cctctgttcc tccctggcag caggtacctg 60 gcagcttcta atgcatagcg agactgtatc gcatgcacca gcagataccg tgtagactcg 120 gccagtatca tggtaagaca ccaccggcct cccaggcagg agcgggagta tggatggcta 180 gtcacagccc gcccccagca tctctgggac caacacctgg aggaataccc tttgagaatt 240 gtggggtccc tggtcctcaa gtgccacggg agtttgcgta agaggggagt tggcagtgct 300 gccctgcagg ttcagacccc catcttgcag aaagccccca tgacctctgc ccattgctgt 360 cccccgcggg gctgtcctgc gctccaggga agctcccgcg cccgcagtgc atgtggggac 420 ccgagaaggg caagcccagc ttgagtgccc gcgggctgcg ccgggcgtga gcggctagcc 480 ccgcacgggc gggcgcgctg tgggcgtggg gaggcgatgc gcgtggcccg gggaaggtgt 540 gtcgcggcgc gcggggggtg tgagcgcgcc tgcccgcccc cgccccgccc agaggccggg 600 caggtgtggg cgggcggcca ggaccccgcc gagccgggct ggagagccgg cgggaaacag 660 gaagcagggg gaggcgcagc cggacggccg ggagggaggg cgtgcagacg gacgcgcggg 720 gtggccgggg gccggacgca cgacccgggg cgggcggcaa tgtggggagg cccgggcagc 780 ccaggaggct gcggggacgg gggcggagcc gggggcgcca cgggcaccgc ccccctgcgc 840 cggcggagcc gccgcccgag tgcggacccg ggagcccgag gcgactgtag cgtgcggggt 900 gagtcgcggg gagctcgggg cgcgcccccg acggcgggtc tgcggacgac gccccggggg 960 tgcttggccg cacatctagc cctagggagc cctggtcgac ccccgtgcgc ctcttgcccg 1020 cagaccctga ggacacggcc atgccgggcc gggcggaggc gggggaggcc gaggaggagg 1080 ccggggccgg ctcggggtct 1100 // ID HSA_3397_ID1 standard; DNA; HUM; 1100 BP. XX AC 3397; XX DT 05-Sep-2005 (Created) XX DE ID1: inhibitor of DNA binding 1, dominant negative helix-loop-helix DE protein XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.20 29655780..29656879 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 20q11 XX CC Database Reference HGNC: 5360; ID1 CC Database Reference ENTREZGENE: 3397 CC Database Reference UNIGENE: Hs.504609 CC Database Reference ENSEMBL: ENSG00000125968 CC Database Reference REFSEQ: NP_002156 CC Database Reference REFSEQ: NM_002165 CC Database Reference REFSEQ: NM_181353 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36617_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:208937_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36619_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36618_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:74752_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:208937_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:208937_s_at CC Database Reference TRANSFAC GENE: G004648; ID1 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: 29655780..29656879" FT /note="Genomic Strand: FORWARD" FT prim_transcript 975..>975 FT /db_xref="dbTSS:ColF1399.seq" FT misc_feature 996 FT /note="SECONDARY ANCHOR: MMU [15901]; Alignment" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [15901]; Alignment" FT prim_transcript 1026..>1026 FT /db_xref="dbTSS:PCD13521" XX SQ Sequence 1100 BP; 245 A; 318 C; 289 G; 248 T; 0 other; gcccgcgcgg cgccagcctg acagtccgtc cgggttttat gaatgggtga cgtcacaggc 60 ctggcgtcta acggtctgag ccgctggttc agacgctgac acagaccggc ccgggaaggg 120 aggggggaga ctgtagctcc gcagctgccg cgccgtggga gggagaccct gctctgaggt 180 ctttgagaag aaaatttaaa aagcagccaa aaatgggaaa aaacattaaa aaatcacgaa 240 ctgttgcagg ttcaggaaat ttttgcaagg agctgcaaat tcaaggtgga atcgaatgca 300 gcctcactcc actgcgctct atctagttca cttcccagcc acccagcccc aaacttacta 360 gactttcccg aattaattgc tcccacccgg gagggatctg ggtaggccct ccgggtctca 420 ggaacacgaa cagcaacatt atttaggaat tgagaaagcc caggggagca gatgtaaagg 480 agcgcccgct ttaaatttcg gtcctgatat ttgtagatca gggtccgaga agcatcttcc 540 aagagggtcc ggaaacccag gctctctggg ctatccagag ccagccgctt ctccgttcgg 600 gcctcaattt ctctcatctg tgaaatggag ctggagaagt gagaaagtga atatgggaaa 660 aactgattcc tgaggtcttt tcattataag gcaatgcctg cttagcttcc ttgcctcctt 720 ccagaggagc ccagtgcggc cctcgcctct acccgctgcc ctgcccggtg ccctgccacc 780 gacccaccct tgctgttctg aaacccgggt cgtctttcca cactgcgagc aggcactaga 840 cgagcaggag gctggaccta ggagcgcggg tcacgccccc atgccgccca ttggctgctt 900 ttgaacgttc tgagcccgcc cctccggggg ccgtggcgtg tttataaaag acaagctgtg 960 gctccgcact ctcattccac gttcttaact gttccatttt ccgtatctgc ttcgggcttc 1020 cacctcattt ttttcgcttt gcccattctg tttcagccag tcgccaagaa tcatgaaagt 1080 cgccagtggc agcaccgcca 1100 // ID HSA_4041_LRP5 standard; DNA; HUM; 1100 BP. XX AC 4041; XX DT 06-Sep-2005 (Created) XX DE LRP5: low density lipoprotein receptor-related protein 5 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.11 67835677..67836776 (FORWARD) CC Score Points: 1 (33.3%) CC Chromosomal Location: 11q13.4 XX CC Database Reference HGNC: 6697; LRP5 CC Database Reference ENTREZGENE: 4041 CC Database Reference UNIGENE: Hs.6347 CC Database Reference ENSEMBL: ENSG00000162337 CC Database Reference REFSEQ: NM_002335 CC Database Reference REFSEQ: NP_002326 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209468_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209468_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209468_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:41831_at CC Database Reference TRANSFAC GENE: G003800; LRP5 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: 67835677..67836776" FT /note="Genomic Strand: FORWARD" FT misc_feature 295..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT misc_feature 977 FT /note="SECONDARY ANCHOR: MMU [16973]; Alignment" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000294304" XX SQ Sequence 1100 BP; 169 A; 371 C; 373 G; 187 T; 0 other; tggcaaagct gtcacaaatc tggaggaaca cacacgttca cgggcactca gttctgtgag 60 gtactgcaag ccctctctga acctgcaagg tggccattgc tgtccccact ttacaaagga 120 ggaaagagtg cgcggagagg ttctacttag acccgccaag ggcacagtcg ttctagaaag 180 tagcagactg ggagttccaa cttgggcttg ctggttccag agccccttct gtgccccttc 240 caggctgtgc ctgggtgaga ttcttctcct accagcacgt cttcttcctg gagggttcag 300 tggctgagct gacaccggtg ggcaagaggc cctggcgggc ttgttgaagg actcaaaggt 360 ggcgtctggg agcctggcgg gactttctcc ctgtcagcct agaggcactt ttagaggagt 420 gtgtctgttt cgcagtcttc gtgtctcata attcataact aaggtagagg gtacacattt 480 agtttacagt aaaacctcaa acccacctcc actcccagcc ggccacttct ctccctgttc 540 ccttctctgc cctccacagg tgagaacaag tgtccggggc cgccccgtgg ggccccaggc 600 tgcccgccct gaaactgcct cgctgtgtgc ccttgggcaa ccccgccctg ctccgtgcct 660 cagtttcccc actcatagag gctccacagg tgacacacct ggctccgggc cccgatcggc 720 cgccgggccc cgcggggcgg aaaccccgcg ccaagcctcc cggaggcacc tccagggcag 780 ggcggggagc gcggggaggg gccgcgggga cctgcgccgc tggggccgcc tggccgccgg 840 ccggctccgg ggggcgcccg cgggagggcg cggccggtgc ggggggcgcg ggtggcggcg 900 gcggggggcg gagacgcggc gcggcttccg ctcccgcgcg cccagctccc tcctccccgt 960 cgtcctggtc cgcggcgccc gaggggggag gcggaggcgc cgggagccgc gcgaggagcc 1020 gccgccgccg cgccatggag cccgagtgag cgcggcgcgg gcccgtccgg ccgccggaca 1080 acatggaggc agcgccgccc 1100 // ID HSA_4067_LYN standard; DNA; HUM; 1100 BP. XX AC 4067; XX DT 06-Sep-2005 (Created) XX DE LYN: v-yes-1 Yamaguchi sarcoma viral related oncogene homolog XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 56953937..56955036 (FORWARD) CC Score Points: 2 (18.2%) CC Chromosomal Location: 8q13 XX CC Database Reference HGNC: 6735; LYN CC Database Reference ENTREZGENE: 4067 CC Database Reference UNIGENE: Hs.491767 CC Database Reference ENSEMBL: ENSG00000147507 CC Database Reference REFSEQ: NP_002341 CC Database Reference REFSEQ: NM_002350 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32616_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202625_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:210754_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:77231_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202626_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:2024_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202625_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202626_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:210754_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:54933_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:210754_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202625_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1402_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202626_s_at CC Database Reference TRANSFAC GENE: G000330; lyn XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 56953937..56955036" FT /note="Genomic Strand: FORWARD" FT misc_signal 937..983 FT /note="TRANSFAC Site R04234" FT prim_transcript 990..>990 FT /db_xref="ENSEMBL:ENST00000276497" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [17096]; Alignment" FT /note="PRIMARY ANCHOR: RNO [81515]; Alignment" FT prim_transcript 1012..>1012 FT /db_xref="ENSEMBL:ENST00000359619" FT misc_feature 1013 FT /note="SECONDARY ANCHOR: MMU [17096]; Alignment" FT misc_feature 1023 FT /note="SECONDARY ANCHOR: RNO [81515]; Alignment" XX SQ Sequence 1100 BP; 250 A; 328 C; 290 G; 232 T; 0 other; agattgtgtc acaaggcagc tgctttgact tattgctctg tagctggggt cagcctcttc 60 agaacattgt taatgagaga aaggaagtgc tttgggcagt gtctggccca tcaggccctc 120 tgtaaatgtt tgctattaat gcaatgctga gatcccagtg aacagaatct ggcttagaag 180 aagtgggtat ccacggtgcc cgagcctaat cttacatctt ggatttgtaa gtggcattta 240 ttgagttgaa catgagcttg agcacgcggt cacacattct ttcagcaaac actggttagg 300 caccagctgc tacgtgcaag cactgcccta catgctggga cgcagctgta gtaggaatga 360 aataacgcca gcattcctgc atgcgggcag tgcgggccct gtacagaaag gtacacgaga 420 taggcatcct cacatccatt gtcctgggag gaaactgagg ctttgagaaa cggagaactt 480 gccgggccat ttgactctac gtcatcccct cccccatcaa tgccctgaac agcctcctgt 540 acacccttaa ggaacttact ttgtaatgat tattaagaac tcagcgagac cccgagcatc 600 acctcggcat atcgcatcct ttctctagag aacccctaat gttggaaggg atcagagcgc 660 acctcctccg ctcctgggag cacccccttc ctaataatac cttggggatg ggtcggaagg 720 aaaggaaagg agacgcgaga ggtgtagtcg atgtgcctgc gaagcccagg ctcctctgga 780 gatccttccg tccgtcccta caggagaagg ctggcccggg ctgctccact ccccggagct 840 gcagactgag tcgccaggtt tctgtgcctt caaagccctg cgcgacggcc acaccaaaca 900 cccaaacctt gggcagggac caaacggtca cttccccgcc ctccgggctc aatatgcaaa 960 tccgagcacc aggaagtagc tgggacctct cggccgagcc cagagacagc cagttcctct 1020 cccgccgcgc cgggccgcgc tgccgctcgc tccccggccg tggcgcctcc gggccagacg 1080 cgctgcagcc tccagcccgc 1100 // ID HSA_4846_NOS3 standard; DNA; HUM; 1100 BP. XX AC 4846; XX DT 05-Sep-2005 (Created) XX DE NOS3: nitric oxide synthase 3 (endothelial cell) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.7 150124795..150125894 (FORWARD) CC Score Points: 1 (33.3%) CC Chromosomal Location: 7q36 XX CC Database Reference HGNC: 7876; NOS3 CC Database Reference ENTREZGENE: 4846 CC Database Reference UNIGENE: Hs.511603 CC Database Reference ENSEMBL: ENSG00000164867 CC Database Reference REFSEQ: NM_000603 CC Database Reference REFSEQ: NP_000594 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:576_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1961_f_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205581_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205581_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:85472_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205581_s_at CC Database Reference TRANSFAC GENE: G003612; NOS3 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="7" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 150124795..150125894" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000297494" XX SQ Sequence 1100 BP; 326 A; 248 C; 324 G; 202 T; 0 other; ccttctcagt ggaccctctc cattgcctcc agagcacagc ttccagtccc caggcggctg 60 cacacatttg caacaaaaca agccaatgta tgaagcaatc ccactcagtg caggagctca 120 acccagcaga ggatccccac agagaggaac tgacctgtgt cttccagagc acacaggttc 180 agagcacaca ggttcattta agtgagaacc cacacttaca gagcaagctg cccaaaaacc 240 acgaccagga gggcccagag aaagagctgt ccccggggcc ttggggacag ggtgacagcc 300 acccagagat catggagaag gggacgtaag gaagacctca cagaggagtc atcctgcgac 360 tgtgttggtt gggtccttca ggaagcagag tcccaggagt tggaagcata agaggaatac 420 tgcgggcaat gcctgagaaa gataacaggg accgggagca ggagtgagtt gggcagggga 480 aggatcaggc ccacaatgcc aggctcacac ctgcagagga gggaagaaga agaagggcct 540 cacatcagcc cagcggggga tgttacgccc acagacgccc cggggctcag ttactgtcta 600 agtgttagaa ataaattttc ggtgccacaa aagaaatagc actcagatat aaatgttccc 660 agcaaggcaa ttttacttct atagaagggt gcatctcaca gatggagcaa tggcaagagc 720 acacctgaac aagggaaggg aaggggtttt tatccctaag gcaggtagcc cctacagctg 780 tgttgttccc ctattggcta gggttggacc acaccgtctg agctaattgt tactggctat 840 tttaaagaga gcaggggtaa gagccggatt ggcagggtaa gtagtttggc aggaaggacg 900 gtcacagaac aggtgactca ggatgactca ggtcagagca ggtgaccagt ggtgactcag 960 ttcggagcag gtgatagaag ctaggagggg gttgtttact gaaactaggg gcaaggagac 1020 gaagagaaca tgaaagttaa actttaagat gaagaacaaa gctgaacata ctgatgcatt 1080 ggatctttgg agaggatctc 1100 // ID HSA_5101_PCDH9 standard; DNA; HUM; 1100 BP. XX AC 5101; XX DT 07-Sep-2005 (Created) XX DE PCDH9: protocadherin 9 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.13 66701862..66702961 (REVERSE) CC Score Points: 1 (5.6%) CC Chromosomal Location: 13q14.3-q21.1 XX CC Database Reference HGNC: 8661; PCDH9 CC Database Reference ENTREZGENE: 5101 CC Database Reference UNIGENE: Hs.407643 CC Database Reference ENSEMBL: ENSG00000184226 CC Database Reference REFSEQ: NM_020403 CC Database Reference REFSEQ: NM_203487 CC Database Reference REFSEQ: NP_982354 CC Database Reference REFSEQ: NP_065136 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219737_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39878_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219738_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:60902_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219737_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219738_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219738_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219737_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="13" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 66701862..66702961" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:CBR08871" XX SQ Sequence 1100 BP; 252 A; 293 C; 338 G; 217 T; 0 other; acttagcaaa gagatgtgcg aagtgtgcgc ctggagacga gccgcctcgg tgacccccat 60 ccgcccgcag cggtggccct ggttccccgg atccgcgccc gcgccctgcg ggtctcccgc 120 gccgcccttg cccgccggac cacccgggct cagagggtcg ctcgctttca gcgcctgcga 180 gcgccgcttc cgcccgggcc tggggagcgc cagcgcgtcc ctcccacgcc ggaccctgca 240 gagcatgctc agtgcacctc atggaacccg gctctcctgg ggccaggatc agatttccgg 300 gttttcgctg ctgccgaggg ggcgcggagg aggggaggct gggagacagt cagcgccttg 360 ttccgcgctc cctccctcgc gccgggctgc ggccgcccgc gccgcaagat gcaggccaat 420 cagagcccgg gggcggggcc tgggcagtca cgccctccct ctgggcttat tgagagttat 480 atcaagaaat tcagttcaga gagaggagag ggagaaggag agaggggcag aggggaaggg 540 agagagggag agcacgcgag acggaaagga gcgcctcaga gtctctgaag cacgcaagag 600 ataaccgatt aggaattttt cgggcaactg tcacccggat agctgtcaga gaatcatcat 660 caccgcaact ctgacgtttc ctacaagaag ttagagactt aagcagtatt ggcatcggat 720 ggaaatggta tgcatgctgc tgtggaaaat atccctgagc tgaagaagtg caactatgtg 780 ttgtgtgtgc taaatgccca gaagaaccca gacccagtgg gtaagagaga cgaaatgtgg 840 agagaatgac taacgacaaa tccgtgaatt tgttctctgg agttgctaat ttgccagccc 900 gaagcaacac attttacaag gaggaaacat tttgctgctt ctgatttctc cccaaactgg 960 tgctaccaga tgcatggctt tctatgtgtt ggaacaaatc attcctaact gcagcatact 1020 gggaaagggg aaaggttgag gcaactaacg taagtgtaaa gtttcgcatg cacaattgta 1080 aattctgtgt ttagatgtgt 1100 // ID HSA_51316_PLAC8 standard; DNA; HUM; 1100 BP. XX AC 51316; XX DT 07-Sep-2005 (Created) XX DE PLAC8: placenta-specific 8 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 84392972..84394071 (REVERSE) CC Score Points: 3 (100.0%) CC Chromosomal Location: 4q21.3 XX CC Database Reference HGNC: 19254; PLAC8 CC Database Reference ENTREZGENE: 51316 CC Database Reference UNIGENE: Hs.546392 CC Database Reference ENSEMBL: ENSG00000145287 CC Database Reference REFSEQ: NM_016619 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219014_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:63342_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219014_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219014_at 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: 84392972..84394071" FT /note="Genomic Strand: REVERSE" FT prim_transcript 982..>982 FT /db_xref="ENSEMBL:ENST00000311507" FT prim_transcript 1011..>1011 FT /db_xref="dbTSS:RCT02058" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 394 A; 205 C; 172 G; 329 T; 0 other; aatgaagtcg cttgtgctaa gtgacatata atcaaactga actttgaaat ggaccagttt 60 tccaaaaaac aggagatttc agtcaacctc agtcagtgta gtaaggaagt cctctctgtt 120 ttagtcctat aaggaaagta actttgaaac aaccaatcta tctttttttc tctgtttccg 180 ctttcttcat actcaccagg acactcattc tattttatag aatgatgtgt tgcttgattc 240 tagaattgca aataaaaggc aattacatct tctaaactaa atttgttgta attttgtctt 300 ttgatagttt aaactatggg atcagaaatt caaagactat gaataaaaat ttcaaaagaa 360 agaaatagta ataccaccaa taagaagaat aattaaaaag gtacaaagaa attggatgca 420 acattgtaaa aagagccata gtttggagct gagctgacat gagctaaaat cctaggtgag 480 taacttgtta gctatgtggc ctctgaaagt cagctcaaga atctgagctt gtttcctcac 540 ctctaaaatt gaaaaaataa ggcctaacta tcaaagtcat taacaagtca ttgataatgc 600 ttggcctatt ttaatgttca gtatctgtaa gttgatacca ttaaaggatg cttgagatgc 660 caactactat ataatctgaa acaataatga tctttttttt ccccacaaag ataacaaaaa 720 acaaacacaa aaaaacaaca gtaagctctg ccagacatgt aaaaccaatc aaactatata 780 atgaattaaa tcctttcccc attaaaaaga cgtatcagtg tacctaacac aatataggaa 840 aagaaacaca ccttatttgg caagagatat attcattctc cagataagag aaacacacat 900 tgaaaccact tctgctggat tactctggcc aataagagcg tctgaaactg ttctatgtac 960 tatgccctgc gatagaaaca cagttacctc tcccctttca cgtagttttc atttgtggtg 1020 agattctctc ccaggccaca agacatttcc tgctcggaac cttgtttact aattgtaagt 1080 actttacaag taagaacttg 1100 // ID HSA_51514_DTL standard; DNA; HUM; 1100 BP. XX AC 51514; XX DT 07-Sep-2005 (Created) XX DE DTL: denticleless homolog (Drosophila) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 208596511..208597610 (FORWARD) CC Score Points: 6 (60.0%) CC Chromosomal Location: 1 XX CC Database Reference HGNC: 30288; DTL CC Database Reference ENTREZGENE: 51514 CC Database Reference UNIGENE: Hs.126774 CC Database Reference ENSEMBL: ENSG00000143476 CC Database Reference REFSEQ: NM_016448 CC Database Reference REFSEQ: NP_057532 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:222680_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:218585_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:47338_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:218585_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:222680_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:50890_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:218585_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="1" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 208596511..208597610" FT /note="Genomic Strand: FORWARD" FT misc_feature 349..>1100 FT /note="ChIP-on-Chip Fragment: HNF1a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT misc_feature 596..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT misc_feature 764 FT /note="PRIMARY ANCHOR: MMU [77065]; Alignment" FT prim_transcript 957..>957 FT /db_xref="dbTSS:TLV00590" FT prim_transcript 977..>977 FT /db_xref="dbTSS:KMR06495" FT /note="Number of reported TSSs: 2" FT prim_transcript 1007..>1007 FT /db_xref="dbTSS:HEP16242" FT prim_transcript 1016..>1016 FT /db_xref="ENSEMBL:ENST00000271754" FT misc_feature 1025 FT /note="SECONDARY ANCHOR: MMU [77065]; Alignment" FT prim_transcript 1073..>1073 FT /db_xref="ENSEMBL:ENST00000318866" XX SQ Sequence 1100 BP; 242 A; 332 C; 274 G; 252 T; 0 other; tgtaacccca aagctccctc tacaccaagc tgctccctgt acggcaacag aactcctgga 60 acttgtccgc agagaatgag cagggccctt gcttttttat ggtcttggcc aggtttagcc 120 tgccttgtaa cccgcaggta acagagctat ggaaatcaaa tgaatcgctg tcaagtcggt 180 gcaagattac tattcagcac atttcatgaa gacctggtct caactgaaca gactgaaaac 240 caatttcaca atttctttgc agtgtctctt agaaactagc cactgtcact gcttagaaaa 300 tcgggggact gctccctcaa gtggtcaaaa cgggcctctc actagagctc gctacttgtt 360 tagccggtat aaggccagtc acacaatcct gcaaatttcc cgcaacctcc cgaaggggtc 420 aaagcccacg ccccagcaaa agcacaggcg ctccccgccc agcgaagaca tgcgcatgcg 480 cctatccgtc ttctcccaaa gcaaccacca cctggtggcg ccacttcccc ccacgcctgt 540 ttcacccatt cagccctctc tttcgaatac ctttgtccaa ttccataagg gcagagttgg 600 catccagttc ctgttcgcca tagccggcat ctgccaggaa agacttagtt gagtttgacg 660 ccatgacccg aatagttact cgactagcct agtcagaaag cttgcaaact ctaccccagg 720 accgccatct tcccccgccg ccttcttgct ggtttttctt ccgcgcgctg tcaagccctg 780 ttacgcatgc gccctggtca ccccgcggtt tgtccgcgcc tctgctaccc cctgcgcagg 840 cgctcaagga gctcttggac tccaggttcc cgcggctggg agaaaaggag gcggggatcc 900 gaagggggaa atgactctga ggcgcccgga cgtcgctcgg aagccaatca gagagcgtga 960 cgtcagtttg gcgcggagtt tggcggccgg ggcttacagt ggcgggagtt ggaggcgata 1020 acgatttgtg ttgtgagagg cgcaagctgc gatttctgct gaacttggag gcatttctac 1080 gacttttctc tcagctgagg 1100 // ID HSA_5367_PMCH standard; DNA; HUM; 1100 BP. XX AC 5367; XX DT 06-Sep-2005 (Created) XX DE PMCH: pro-melanin-concentrating hormone XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.12 101093979..101095078 (REVERSE) CC Score Points: 1 (100.0%) CC Chromosomal Location: 12q23-q24 XX CC Database Reference HGNC: 9109; PMCH CC Database Reference ENTREZGENE: 5367 CC Database Reference UNIGENE: Hs.2182 CC Database Reference ENSEMBL: ENSG00000183395 CC Database Reference REFSEQ: NP_002665 CC Database Reference REFSEQ: NM_002674 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206942_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206942_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206942_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:32005_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="12" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 101093979..101095078" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000329406" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: RNO [24659]; Alignment" XX SQ Sequence 1100 BP; 427 A; 177 C; 154 G; 342 T; 0 other; aaacatatgg gaagacactt aacctctttg gtaattagga aaatacaaat taaaaggaca 60 atgagacaca agagtcagct aggacatgga acaatggaaa ttctcatacc ctgcttatcg 120 agggcacaaa tcgcttacaa ctatgttgga aaacattttg gcattagtaa agctgaacat 180 atacatactc catgatccag taattccata ctgagaaata tactctagaa aaattcttac 240 atatatgtac cagaagacat ataaaagaat gtattatctt attcattggg gtcaaaatta 300 gaaattaact ctgaaatgtt taattaaaag tcatacaaca taaactcatc atccaaaagt 360 aatgtttatg ggcacataaa tattcttttc atggactaat tcattaattt ctaaattcat 420 taataaatat ttgtacatat tatccttttg taaatgcaga gataaaatac acctgacagg 480 tcaatttttg atatagcatg aatggctttt tgttcacact gacaggcata tgtactttaa 540 tcaccaaaaa ctatatcaag tatttataaa agaaagtctc ttttgaggat tatttcagtt 600 taatcaggat taaaaggaaa taaaacttta tccttatcat ccttgagtga aataacttga 660 gttttaatat ctttacttaa tcagaaaata cacaaaagga aacaataata tagagagagc 720 ctgatgtcct gtggtcttcc ttaataacaa cccattttca agagactata atctactcaa 780 cagaaagcat tctaccaagg atcttagtca gattctgaga aaattcacac tcaaaataaa 840 caatgtgtca ctaaaaccaa aacaatgtag gtattagcag ctgcataaag gttagcctca 900 atctaatgag tcatttctaa aatgatgaaa agtataattc tttgaagtgc tttctattca 960 agctagaaaa tatataaaga tacagaatcg tttaccaagc aggctgacag agaaattttt 1020 cattttcttt cttgtttgac tgtatgcaaa catcaaacta agaatggcaa aaatgaatct 1080 ctcttcctat atattaatac 1100 // ID HSA_54345_SOX18 standard; DNA; HUM; 1100 BP. XX AC 54345; XX DT 06-Sep-2005 (Created) XX DE SOX18: SRY (sex determining region Y)-box 18 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.20 62173281..62174380 (REVERSE) CC Score Points: 1 (33.3%) CC Chromosomal Location: 20q13.33 XX CC Database Reference HGNC: 11194; SOX18 CC Database Reference ENTREZGENE: 54345 CC Database Reference UNIGENE: Hs.158654 CC Database Reference UNIGENE: Hs.8619 CC Database Reference ENSEMBL: ENSG00000196700 CC Database Reference REFSEQ: NP_060889 CC Database Reference REFSEQ: NM_020713 CC Database Reference REFSEQ: NP_065764 CC Database Reference REFSEQ: NM_018419 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:55872_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:221869_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:55872_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:55872_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:73049_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:221869_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219568_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:67286_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:54058_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219568_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:219568_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:62957_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:55872_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:221869_at CC Database Reference TRANSFAC GENE: G006748; Sox18 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: 62173281..62174380" FT /note="Genomic Strand: REVERSE" FT misc_feature 627..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000340356" XX SQ Sequence 1100 BP; 254 A; 337 C; 357 G; 152 T; 0 other; gggaggacac tgccctgcac aggacgcaca caagaccctc tccccacctg ccctcacagg 60 cagagccgcc ccaggtgatc tctgaaggtc agccaagctc ctctcctggg gctgacccac 120 cagggccaaa cccaagcact gcccaacccc agggaggggc cttgtccaca gcagtggaaa 180 cgggtcaaac atgggggaca ggggcccacc aggagtaacg gctgaggaga acaagatggc 240 aaaaagaaac atttaataat gagggggaaa gggcagaaag gtgcaatcca ggcaggcagg 300 ttgagggcag gacatgccgc cttctagggt ctccagagaa gctgtgtcaa cggaggacgt 360 gggccgggga gggcccaagg ctgcagcaca tctacacgag gggtcagcag aactgcgaga 420 aagggggtga ggcctccagc cttgtggcca catgagatcc cccagagtgg aaggccgcac 480 aggctcaccc aaggctgggc tctccaccca ccatgcccaa gactcccagg aggctggttg 540 ggcagggcca tccccagttc acaccacaga ccccacagag gctgagacac cccacctcca 600 gagaatggag ctgggagggg cagcctgagc ctgctcaccc accttccagc ggtttccaca 660 ctcgttgcag acaacaaagg tggtcatggg ctcatcagag ctgcgggtct gcacctgtga 720 acagggctgg gtgaacccag ggtcacctcc atgctccgct gcagacggca tcccctcaac 780 atgggcagtg cgggcctcgc agccactgag ctcccacagg tgacctgatc cgaggccgcc 840 tcgtgactcc aaccttccaa agctgagcct ccgggggagg gagacagagt ttatcggggc 900 agaggccctt gtgtgagcct gaagcagctc acattggctg gggaccagga gggcccagac 960 ttggctgagg gcaagagggt cccaatggtg gggggaacta gcaggggtcc ccagtgcccg 1020 cggctgcctt ccggaaggcc caagggtgag cctccggcca caggcagagc ctgttctgac 1080 cagtggctgg gagcaggaga 1100 // ID HSA_54873_PALMD standard; DNA; HUM; 1100 BP. XX AC 54873; XX DT 07-Sep-2005 (Created) XX DE PALMD: palmdelphin XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 99822663..99823762 (FORWARD) CC Score Points: 8 (80.0%) CC Chromosomal Location: 1p22-p21 XX CC Database Reference HGNC: 15846; PALMD CC Database Reference ENTREZGENE: 54873 CC Database Reference UNIGENE: Hs.483993 CC Database Reference ENSEMBL: ENSG00000099260 CC Database Reference REFSEQ: NP_060204 CC Database Reference REFSEQ: NM_017734 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:222725_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:218736_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:218736_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:232187_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:222725_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:48956_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:218736_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:232187_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: 99822663..99823762" FT /note="Genomic Strand: FORWARD" FT misc_feature 337..1055 FT /note="ChIP-on-Chip Fragment: HNF4a_hep" FT /note="PubMed:14988562" FT prim_transcript 883..>883 FT /db_xref="dbTSS:LNG01909" FT prim_transcript 957..>957 FT /db_xref="ENSEMBL:ENST00000263174" FT prim_transcript 983..>983 FT /db_xref="dbTSS:HRT01671" FT prim_transcript 1027..>1027 FT /db_xref="dbTSS:HEP01715" FT prim_transcript 1028..>1028 FT /db_xref="dbTSS:CAE09426" FT /note="Number of reported TSSs: 2" FT prim_transcript 1041..>1041 FT /db_xref="dbTSS:SLV03372" FT prim_transcript 1055..>1055 FT /db_xref="dbTSS:HRT05939" XX SQ Sequence 1100 BP; 324 A; 249 C; 245 G; 282 T; 0 other; tcaatgtttg ggttgtcctt ttaacctctt cagctgaatg ttgatatgaa agcgcttaat 60 agcattcaaa cacataataa taaggtagtt ggtaattagg atttacttca gcaaaattta 120 attaaagaac ctgtagggaa aagaaaacag acagagccaa ttgtacagct tcccagcctc 180 tgctttgacc taagagtctc actgggcttg cctgcctttt tctaaaggat gggcgaatat 240 tcacacagtg ccgggctcca ggcagttacc aaatgtctca tcacattttc aaaggctcac 300 tcctctctct tgcgtaaccg gtgaggtcaa aatgggcacc ttcctgaaag ccaagagtgt 360 catttctgaa cagcgtccaa gaaagaaaac tgcattccat agaaatccaa gtcaagcaat 420 aacaaaaggt ggcacttggt gcttaagcca cactaaatac cttggtgggc caacttctta 480 atatagtcac attaacacct ttgatttctc catgacctaa agattccaaa gtttgcaaca 540 aagtgctgag caggggggtc gggggtgggg tgtagacggg ggagaacgaa ccaatgtaaa 600 tttaccacta catgaagttt aaagtagcta tagattgttg tattattatc aaatccaatc 660 agtggaagaa aggcaaacaa gtgacttggc acttctgcct cagtcaaggt aaggctctct 720 cccctagagc tagcaagcag gtaaacgagc tttgtacaaa cacacacaga ccaacacatc 780 cggggatggc tgtgtgttgc tagagcagag gctgattaaa cactcagtgt gttggctctc 840 tgtgccactc ctggaaaata atgaattggg taaggaacag ttaataagaa aatgtgcctt 900 gctaactgtg cacattacaa caaagagctg gcagctcctg aaggaaaagg gcttgtgccg 960 ctgccgttca aacttgtcag tcaactcatg ccagcagcct cagcgtctgc ctccccagca 1020 caccctcatt acatgtgtct gtctggcctg atctgtgcat ctgctcggag acgctcctga 1080 caagtcggga atttctctat 1100 // ID HSA_55388_MCM10 standard; DNA; HUM; 1100 BP. XX AC 55388; XX DT 07-Sep-2005 (Created) XX DE MCM10: MCM10 minichromosome maintenance deficient 10 (S. cerevisiae) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.10 13242591..13243690 (FORWARD) CC Score Points: 6 (85.7%) CC Chromosomal Location: 10p13 XX CC Database Reference HGNC: 18043; MCM10 CC Database Reference ENTREZGENE: 55388 CC Database Reference UNIGENE: Hs.198363 CC Database Reference ENSEMBL: ENSG00000065328 CC Database Reference REFSEQ: NP_060988 CC Database Reference REFSEQ: NM_018518 CC Database Reference REFSEQ: NP_877428 CC Database Reference REFSEQ: NM_182751 CC Database Reference AFFYMETRIX: AFFY_HG_U133B:223570_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:220651_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:69475_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:220651_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:76057_f_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:222962_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:222962_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:223570_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:220651_s_at XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="10" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 13242591..13243690" FT /note="Genomic Strand: FORWARD" FT prim_transcript 997..>997 FT /db_xref="ENSEMBL:ENST00000357807" FT /note="Number of reported TSSs: 2" FT prim_transcript 1001..>1001 FT /db_xref="dbTSS:TDR09531" FT /note="Number of reported TSSs: 2" FT prim_transcript 1004..>1004 FT /db_xref="dbTSS:HKR01582" FT prim_transcript 1005..>1005 FT /db_xref="dbTSS:OFR08577" XX SQ Sequence 1100 BP; 304 A; 233 C; 305 G; 258 T; 0 other; ctgagccaat ataggtttaa gtaatagggc tgagctcata aatggagcag taatattcca 60 ttaggacaca gaaaaaagtc aacgtagatg gcatcaggac tgtttatctt cagtcttcct 120 aaagtcgatt ttaattgttc tgaaaatgaa agtacgtagt ggatagagat aggatcttat 180 accaaaggga ttattagtgg gggaactgca gtgcctgaac agtgtctgca aggaggaaaa 240 ggggggaaag acttaaagtg gccatttggt ccatcaaagt ctcttctgct atcaatccct 300 tgaaattatg taaaagctaa atgttattct gcatttagaa actatgttct tagtattatg 360 tacaaacact attttttaga atgtaaatac ataaagaggc ctgaatttta ctgaaaaaaa 420 aatctgtgaa agatatggtc tgctgataag ttctcttcag ccctgacgcc ccttagaagt 480 cccaaaatct atggaacagg aattactcgg gaaatggtgg tttcagtgta aaagatgtca 540 tctacccttt ccctcactgc acagatggtg aaggggaaac tcagagagat aagtcacttc 600 cccaaggtca gacagggtaa aagtggaccg gatctgtttg gtcctgagcc caaacatttc 660 gaatggacat aaggctgaca aaggaacagt cggtcccaga gcgtcaggag ttgaggtggg 720 atgggaccgc agggaaaata ctgggtggga tgacttaaac ttcccggcac cagggggcgc 780 cagacactct attttaccta aaggagactg gcttctaccg acaggaaggt cccttgcccc 840 caacaaagag ggcgtccaat gacgtaaacc aatccgattg ctctgtgcca gggccgggat 900 tcgctggcgt agccagtcag tgctgcccca cagccgcgtg cgtctgacgt caaggcaggg 960 gcgggatccg gttggaattt tggcgggttc agctgtgaac gaagaaggcg tcccggcatc 1020 gggtgaggag cgcgggcccc gggcgtgcgt gtgaccctcg ggcggcgggg ccggggccgc 1080 ctcgcacgtc tctgcgcggg 1100 // ID HSA_5567_1_PRKACB standard; DNA; HUM; 1100 BP. XX AC 5567_1; XX DT 06-Sep-2005 (Created) XX DE PRKACB: protein kinase, cAMP-dependent, catalytic, beta XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.1 84254792..84255891 (FORWARD) CC Score Points: 5 (13.2%) CC Chromosomal Location: 1p36.1 XX CC Database Reference HGNC: 9381; PRKACB CC Database Reference ENTREZGENE: 5567 CC Database Reference UNIGENE: Hs.487325 CC Database Reference ENSEMBL: ENSG00000142875 CC Database Reference REFSEQ: NM_002731 CC Database Reference REFSEQ: NM_207578 CC Database Reference REFSEQ: NP_891993 CC Database Reference REFSEQ: NP_997461 CC Database Reference REFSEQ: NP_002722 CC Database Reference REFSEQ: NM_182948 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202741_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202741_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:202742_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:84201_r_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:235780_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:46322_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202741_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:202742_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:202742_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36215_at CC Database Reference AFFYMETRIX: AFFY_HG_U133B:235780_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: 84254792..84255891" FT /note="Genomic Strand: FORWARD" FT prim_transcript 975..>975 FT /db_xref="ENSEMBL:ENST00000360848" FT prim_transcript 992..>992 FT /db_xref="dbTSS:CBL00703" FT /note="Number of reported TSSs: 3" FT prim_transcript 1057..>1057 FT /db_xref="ENSEMBL:ENST00000362059" XX SQ Sequence 1100 BP; 259 A; 330 C; 315 G; 196 T; 0 other; acaggtattc ataaaacacc tactatgcct ggtgccttgg gaacatagaa taaattggga 60 agttacagtc tattttgaat ttggaataaa tggaaaacac agagcaaagt tcaatggaac 120 atgcaacaac aaaaatgcta gagtgccaca taatttacct aagtaaagct aacagcaaaa 180 tcaagtactc taagatttat attaataaaa acgcaactaa caattggtaa tgtatttatt 240 ttcagatcta cacagaagtt gctaaataca atgctgtaca tcaacagaag ttctgcagaa 300 atagtaaaat tttcctttat ctccacctgg gaagtctgaa aacatcatag ggcttgtgac 360 tggggcctaa taaccccgag gacaacgtgg tgggctgagc gaatacctca atgtgcgaga 420 gaacgaaaag ctcgaaccac gaccgtgcct agggaccagg cttttcctgt ggccgatgcg 480 gggcagatgc agacccagag gccacccttg cgcgcgatct ccaacccgac ggtgcggctc 540 ctctcggacc tggagctgtg gggagaaggc agccttttag tgaggagccg ccgcgtggcg 600 ggacgcaagg aaaaccaccc gagccgctga acagtattcc gcgactgcac tccagggcac 660 cgggaccgcc agggtgagga gggactctgc gttctgcaaa gctagcggtt cccactccac 720 ctcccactat ctcagcgatg ggcacgcgag cgccagcccg ggcgaccgcg ggggaagaag 780 cggtccacgc cacctcaggc ccccgcccca ggctctgcca gctgggggtc caccgcccgc 840 ccccggggtc ccgggcctgc gcgtcacttc cggcgcgcgc gcccgcctgc gaagatacag 900 tcgggccagg gcctggcctg ggcgcgcggc tgcccggggg cgcgcagaga gggcggaccg 960 cgcgaagggg gagtgtctgc ccgccgccgc cactgctgct gccaccgccg tcgccgccgc 1020 cgccgccgcc gccgctgctg ctgccggtgc taaggagttc gctggagccc tttcctcaga 1080 cccggcccgg tcttcgcgcc 1100 // ID HSA_57211_GPR126 standard; DNA; HUM; 1100 BP. XX AC 57211; XX DT 07-Sep-2005 (Created) XX DE GPR126: G protein-coupled receptor 126 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.6 142663811..142664910 (FORWARD) CC Score Points: 2 (100.0%) CC Chromosomal Location: 6q24.1 XX CC Database Reference HGNC: 13841; GPR126 CC Database Reference ENTREZGENE: 57211 CC Database Reference UNIGENE: Hs.318894 CC Database Reference ENSEMBL: ENSG00000112414 CC Database Reference REFSEQ: NP_065188 CC Database Reference REFSEQ: NP_940971 CC Database Reference REFSEQ: NM_020455 CC Database Reference REFSEQ: NM_198569 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36014_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213094_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213094_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213094_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: 142663811..142664910" FT /note="Genomic Strand: FORWARD" FT prim_transcript 949..>949 FT /db_xref="ENSEMBL:ENST00000296932" FT prim_transcript 1052..>1052 FT /db_xref="ENSEMBL:ENST00000230173" XX SQ Sequence 1100 BP; 207 A; 365 C; 316 G; 212 T; 0 other; agctaatcag cttgaaataa ttgttagggc acttctgtgt atggcctgtg catgtgccag 60 tgtgtacacc gtgcaagctg agctgttgag gttctggatg tgcatacagc cctggcaccg 120 gaaggtttgc ctctagcatt ttgtggacta actctggcag tacacaatgg gaagaaaacc 180 tctttccaag tgtgagccct tctctcttct cattcccaag gaggtgtgtc cagatccctt 240 tgccagacag ctactttaca ggagcattgg agagcaggca gctaactttc cccaacaagc 300 agctggattt acgttggcaa atcaatccct ctcaataaaa tgttatgtga ccatcttccc 360 agccccccgt taaaatccct tcattttttc gagcaagcga actagtcaga gaagacagaa 420 aagttaagta aagaaagtgg cagaaaagtg aagcaaagca acagcccggg agcgtggcgg 480 ggggacccgc gcggggactc gggtaggctg caaacgctgg ggagatgcca caggagcgcc 540 tgccttccca gcttctcctt tctctcgccg agggtctctg gggttcagcg ctcccggcgt 600 ttcggcgacc tccgggtccg ccctgtcccc tcccagctgg ggagctgagc ccggctctgc 660 gcccatcgcc gaccccggcc actctccctt cgctgctcgc tccaaaagcg cctgtcccgc 720 cccgcggggc gacttctccc tttcggccct ggggttgaag atcctgtgtg gggcagctgc 780 gccttcggga cagccccagc cgcggagcgc ccagaccagg gcagccggag tcgggtcata 840 cgccgcacgc cgccggggcc gccgcacctg agcccagctc cagtcacgcc ggaagcgcgg 900 gcggagcgca cgggtccggg gagagtcgcc tgcgcccgcg agggggaccc aagtacctag 960 ggtggtggcc gagtcccgcc tcccgccagc gggggcgagg acctgcgacg cgcacccctg 1020 cctggcccgg tctcctcagc accagcccca cgcacaccct acttcctcag cttctcgccc 1080 tcaccctgcc aacttccctg 1100 // ID HSA_6505_SLC1A1 standard; DNA; HUM; 1100 BP. XX AC 6505; XX DT 05-Sep-2005 (Created) XX DE SLC1A1: solute carrier family 1 (neuronal/epithelial high affinity DE glutamate transporter, system Xag), member 1 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.9 4479478..4480577 (FORWARD) CC Score Points: 2 (66.7%) CC Chromosomal Location: 9p24 XX CC Database Reference HGNC: 10939; SLC1A1 CC Database Reference ENTREZGENE: 6505 CC Database Reference UNIGENE: Hs.444915 CC Database Reference ENSEMBL: ENSG00000106688 CC Database Reference REFSEQ: NP_004161 CC Database Reference REFSEQ: NM_004170 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:206396_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:206396_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:213664_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38267_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:38268_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:213664_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:213664_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:206396_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: 4479478..4480577" FT /note="Genomic Strand: FORWARD" FT prim_transcript 963..>963 FT /db_xref="ENSEMBL:ENST00000262352" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [20510]; Alignment" FT prim_transcript 1039..>1039 FT /db_xref="dbTSS:KAR03048" FT misc_feature 1050 FT /note="SECONDARY ANCHOR: MMU [20510]; Alignment" XX SQ Sequence 1100 BP; 239 A; 338 C; 333 G; 190 T; 0 other; tgataagaag accgcttaca gctgcggagg tactgatttg gtaaagggag ggaaagagat 60 tgtatacgtg agagtgaaaa aattgggtag aaaaatggaa gagcatcaga aattcactta 120 gcaacaccaa atatatttgg caccactaac ctagtttctc ctgtgtttgc ctttccaatc 180 cgttggacct taggggatgg accgcccact ttctccccag agcggctccc gggtccggtt 240 ctcagttcta atcactgccc caagcctcca tgctccaggg cctgtggtca cagagcaagt 300 cccaaggagc agaagtaaag ttctaagaga aatcaccatc tccttgtgca gggaacactc 360 ccaagcccag tgtccacaga caaatcacct ccagcgactc gaagaggaga ataatccctg 420 tgggggcact ggaggctccg cgtgaaagtt tccaaagcca tgttctgccc caggactcct 480 ttctctcctc ccagaagctt caggctttcg cggctgctgg cacatcccag cctgagtagc 540 cgagcaagag ggacccaagg caggatcagc ttcccccgac ttgaaagggc acccgttctg 600 caggtgccgg cgctggaaat agctggtgtg gagaacggag agggagacgt gcaggatgaa 660 gtccgcgccc aggagggcag tggctccgcc tctctgggtt agggacagaa gaaaaccctt 720 aacccaaagc cctagcatga gtgaggcgtg gaaagcgaga cagactccag tggaaggctg 780 tggggcggga ctcagggttc ccggagaggc cgccccagct cctgccgcag cgctgggcgc 840 cctaccacgc ctgctcccta gggaccccgg gcgtcccacg cacgcaccca ccctccttcc 900 cgggcctgcc gctcctccct ccttcctcgc tggttggccc aggcgccgca gagcgcggcg 960 gcagcaggag gagccgggcg cgcctgccac gcaaaactac cgggctggca gggcggcggg 1020 cgcggtgcgc gatcccgggt ggcggcggca acggcggtgg tgacggcggc gactgcagcg 1080 gccggctctc acctctcccc 1100 // ID HSA_7026_NR2F2 standard; DNA; HUM; 1100 BP. XX AC 7026; XX DT 06-Sep-2005 (Created) XX DE NR2F2: nuclear receptor subfamily 2, group F, member 2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.15 94669400..94670499 (FORWARD) CC Score Points: 2 (25.0%) CC Chromosomal Location: 15q26 XX CC Database Reference HGNC: 7976; NR2F2 CC Database Reference ENTREZGENE: 7026 CC Database Reference UNIGENE: Hs.347991 CC Database Reference ENSEMBL: ENSG00000185551 CC Database Reference REFSEQ: NM_021005 CC Database Reference REFSEQ: NP_066285 CC Database Reference AFFYMETRIX: AFFY_HG_U133B:229092_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:229092_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:215073_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:215073_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209121_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209120_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209121_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:47529_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:215073_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209120_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209121_x_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209120_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:39397_at CC Database Reference TRANSFAC GENE: G004656; NR2F2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="15" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 94669400..94670499" FT /note="Genomic Strand: FORWARD" FT prim_transcript 881..>881 FT /db_xref="dbTSS:WMD05712" XX SQ Sequence 1100 BP; 290 A; 244 C; 239 G; 327 T; 0 other; atcttaccat aacagtttcc taaaataaaa gatccgtgtt tccccattat tcttctctta 60 aaacaaaaca aaacaaaaat ccattagtta agacagtatt aaactgtgag aggcagcata 120 gtttatattc aattttcact agttaccgta ttcttgcttc ctttattcgt tttggggagt 180 agagaaaggg agggggtgaa tgaagcattc attatctgaa ggcatggaat ggggaacccc 240 tccccccaaa agaaatagat ttcctcctca ggaaagttct agaataagga ccggaaaggg 300 gggaggcaga aatccacagg ggagaggggg aaaaatcact tggggagact tgagttaaaa 360 gtagaaaatg aggattccaa aggattccta ggaaaaatgt tgccctcttg tctcaagttc 420 tatctttgat ccaggacgag ggaagcctgt ctgccagtct gcgaggctga tgctttttcc 480 ccctcctctt ccacctctgt tttttcccaa cttgctttag gattagcctc catctctctc 540 gaccccaaac agtggaattt ggctgtgcct tgggtcgtct tgctttgcaa tatcgcctat 600 agttgttggc ggttttctgc tgaggctgag ccgtttgctc cagcctccga ctaaactcat 660 taagttggga gatttttttc aattggacgg gtgtttttaa agtctcgtct ttccagcccc 720 aaacaaggtg taacaacgca ctcttccttc taaggaatga gatgagagac aaggatcact 780 ccagacatct cctacctacg gtttggggtt ttttttctta aaggcgaggc ttgcattcct 840 cagcagctat gtacaaagct ccctgaaacc ttgtctctct aaagttagtg tgcagggttt 900 tccaaggctg agagagccta atacatgggg aagcacttcc ttgaggtgga agatctctcc 960 cttcaccttt cctctttttc cctgcaggct agtgcctact ttttatcagt ttgcacaatc 1020 gcttagataa acaccgagga ggagattctc tttaattatc aaagacacat cttttcaggg 1080 ggccaacaaa gcatttattt 1100 // ID HSA_79633_FAT4 standard; DNA; HUM; 1100 BP. XX AC 79633; XX DT 07-Sep-2005 (Created) XX DE FAT4: FAT tumor suppressor homolog 4 (Drosophila) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.4 126671696..126672795 (FORWARD) CC Score Points: 2 (40.0%) CC Chromosomal Location: 4q28.1 XX CC Database Reference HGNC: 23109; FAT4 CC Database Reference ENTREZGENE: 79633 CC Database Reference UNIGENE: Hs.269121 CC Database Reference ENSEMBL: ENSG00000196159 CC Database Reference REFSEQ: NM_024582 CC Database Reference REFSEQ: NP_078858 CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:219427_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:219427_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:52451_at CC Database Reference AFFYMETRIX: AFFY_HG_U95C:63809_at 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: 126671696..126672795" FT /note="Genomic Strand: FORWARD" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000335110" FT /note="Number of reported TSSs: 2" XX SQ Sequence 1100 BP; 371 A; 159 C; 176 G; 394 T; 0 other; tttttcttag ataaatcact tgacatttca gtgccttaat tttgactctc tgtaaaataa 60 cagaaatgga atggaaatgg acttgatgat atttaacatt cctacaaaaa gtattagtat 120 gttgacttgc aaatgaatgg atttctgaac tttcagtgta ctacaaatcc tacggtctcc 180 caaaagaaaa caaaagattg tttttcttct ttatttgaga accattttat gtagattgca 240 ggaaggttgt gaattaaaat atgtttagat tttttcattc cgttcattaa gaaacatttg 300 atttaagctg cagagaggat atgcatttaa gaatatgttt agaattgtgg ttgaggtggc 360 aaccaccatg caattatcag tttattaaca ggggaatgaa ctcataatgg actttgctat 420 tttagtcatt tcctttaact tgaatataat cttctacttt cataatatca atttaaattg 480 gggaaatagc atgttttatc attagatcca caaatatata atggtttgat attagcgatt 540 gttaggtaat gattgttcct tagttatgta gttgtatgct gaaacattta aaaaattaat 600 ccccatgtat aataacattc ttgatgtaga gcaaaataaa atgatagact gcatattata 660 aaaaaaagag aaaagcatta tattatttta tgcactattc ccacagaaat attttttagt 720 tttaaaatat ccatttgacc cttcagcaag ctgaatacca gggattttat tccttcagca 780 taaagtaatt tggtaacaat atttaaaggc atatttctaa cttaaatttt acttttataa 840 aattaccaaa agacagatca tttgtgaact aattggttat tagctccttt aatctcagtc 900 atgtgtttgt ctctaaataa aattatttca tttaccagag ttttactgct cagggctcag 960 gtgactcagt caagaaagtc attcttgtga agctacctaa atggtaacaa cggtagtggc 1020 agtgggtgat accttagctc aaccattagc tgcagctgaa gtgtttattg taagtcaagc 1080 acagatctac caactacatt 1100 // ID HSA_862_RUNX1T1 standard; DNA; HUM; 1100 BP. XX AC 862; XX DT 06-Sep-2005 (Created) XX DE RUNX1T1: runt-related transcription factor 1; translocated to, 1 DE (cyclin D-related) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 93176520..93177619 (REVERSE) CC Score Points: 1 (33.3%) CC Chromosomal Location: 8q22 XX CC Database Reference HGNC: 1535; RUNX1T1 CC Database Reference ENTREZGENE: 862 CC Database Reference UNIGENE: Hs.368431 CC Database Reference ENSEMBL: ENSG00000079102 CC Database Reference REFSEQ: NM_175635 CC Database Reference REFSEQ: NM_175634 CC Database Reference REFSEQ: NP_783554 CC Database Reference REFSEQ: NP_783552 CC Database Reference REFSEQ: NM_175636 CC Database Reference REFSEQ: NP_783553 CC Database Reference REFSEQ: NM_004349 CC Database Reference REFSEQ: NP_004340 CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:216831_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205528_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205529_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205529_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35641_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205528_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:216831_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205528_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35638_at CC Database Reference AFFYMETRIX: AFFY_HG_U95E:91343_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205529_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:216831_s_at CC Database Reference TRANSFAC GENE: G018247; RUNX1T1 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 93176520..93177619" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000360348" XX SQ Sequence 1100 BP; 219 A; 308 C; 273 G; 300 T; 0 other; tcacctgtgg ctaccaatca caagtgttcc tccttatcac aatgatgctg gctgcaggag 60 tcttcagctg ggacacatta aagttcaggg acagaagcta ttttatatct ctgagtgtgt 120 gaatgtgcag gggctggaat ttaggagtat tggggttagc aaagaaaggg acaagaactc 180 cgacttgagg ttggtctgga aggcagctta actgctctat agactcagta ggtttgtttt 240 gcaaaatgtg gctgtttgga tggaggtgag atggcgactg tctccttagg ctctgccaaa 300 agagagctct tgatcctcct ctgaccttga cagaatctcg aacatgttcc agcctagccc 360 tggagcaggg aaatacagtt tgctggattc ctcccttctt tgggtggtag gggcagattt 420 gggcatgcag gcgacttcta gcctgcctct cattcccaga tagccttagg gtagctctcc 480 cccactttct ggccccatcc tggggtctga gcccccgccc cctcctccat ccctccttcc 540 ctcctgcctg tgtctctcct tccctcctgc ctgtcccttt ctgtcttctc tctctctctc 600 ccacttttcc tccctctccc gctccgtctc acacgcaccc tctgtttatt ttcctgcctc 660 catctgggcc ctgctgatat tgtaatcacc ctgatgcacg ttggcttctc tcctctccct 720 cctgcgctca cacactcact cacacacaat gtgccatcct gacaaggctt ttacttctga 780 taagctccaa tgtgtgttta atgaatacaa agccgcggtc tgggtgccgc ctcggccgcg 840 gccgctctcc cgcgctcctt tgccagaagg taatctccgt gaacagggga gggaggcgag 900 cagggaggaa ggaggggtgg ccaggaggaa ggggggcgtg gggaggcggc ttttctctct 960 ccctctctcc ctttccaaat gattcagaag tcgataagac caggagaagt gaagatgtaa 1020 catgttatct gtcgctcctc ttagctggcg gagagaattt acatttaaag attagcagag 1080 tgagaaagag aaatctgcct 1100 // ID HSA_9134_CCNE2 standard; DNA; HUM; 1100 BP. XX AC 9134; XX DT 05-Sep-2005 (Created) XX DE CCNE2: cyclin E2 XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.8 95976561..95977660 (REVERSE) CC Score Points: 2 (100.0%) CC Chromosomal Location: 8q22.1 XX CC Database Reference HGNC: 1590; CCNE2 CC Database Reference ENTREZGENE: 9134 CC Database Reference UNIGENE: Hs.408658 CC Database Reference ENSEMBL: ENSG00000175305 CC Database Reference REFSEQ: NP_477083 CC Database Reference REFSEQ: NM_004702 CC Database Reference REFSEQ: NP_477097 CC Database Reference REFSEQ: NM_057749 CC Database Reference REFSEQ: NM_057735 CC Database Reference REFSEQ: NP_004693 CC Database Reference AFFYMETRIX: AFFY_HG_U133A:205034_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:211814_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:211814_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:205034_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:205034_at CC Database Reference AFFYMETRIX: AFFY_HG_U95D:82614_g_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:35249_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:211814_s_at CC Database Reference TRANSFAC GENE: G003817; CCNE2 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="8" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 95976561..95977660" FT /note="Genomic Strand: REVERSE" FT prim_transcript 1001..>1001 FT /db_xref="ENSEMBL:ENST00000308108" FT /note="Number of reported TSSs: 2" FT misc_feature 1001 FT /note="PRIMARY ANCHOR: MMU [12448]; Alignment" XX SQ Sequence 1100 BP; 166 A; 328 C; 454 G; 152 T; 0 other; ggcgggcccg gggcctgcac gtggtggcga tctttcttcc cacccggcca ggtccccggg 60 gaccaccgcg ctcaggggga ggaggaatgc cgttcccggg ccccgctccg gagaggggtt 120 ttaccctctg ggatcccgga attggaggtg gagaagagag gaagcaaggg agggcgcggc 180 gtggcgcgag cgtttcctgc gcggggactg cggggtggca gctggaggcc actgcagggg 240 cagagcggcg ggttggggga gcgaccgacc catggggagg gaaacccggt agggggagca 300 gggagccgga aagcagggtt gatacatacc tgggtgggcg ggctggaaat gccttccctg 360 ggcgcgccgc gcaaggccgg cggagcgggc tccgggtggt cgcggaccgg gactggggag 420 agcagagccg cacttggcca ggcgcgtggc tgagtggtgt ttacattctg cagccactcc 480 acgttgtgct gccgcccgtg cctcccattg gccagctctt cagccaacgc tttgctcctc 540 cccgaggggc gggccctcgg gtccccgcgt cgctcaggaa agacctgggt tccctgaggc 600 cttggcggga cagctagggc gcgcccctgg acggtcactt cccagccacc ctatggtcgc 660 ccgagtcgtg tccccctgtt atgcgcccgg gctgagccgc aggctgacac ccccgaaatc 720 caggagttgc agtgggagga agcaaaagca aactggcggg agatgcgcga gccaggcggc 780 ggggagaaca gccgcggaga aggagcccct gagagtttcc ctaccgccgc cggccgcgcc 840 gtggagcgcg gtggacgcgg gcagaaggcc cggtagagtg gaccccacgg ccgctccggg 900 tggcgggcgc gcactgagag cagggcgcgg cgcgcgggca cgcgggcgga cgggcgggag 960 aggggagcgc gctgtccgga ggtgtcagtc tgaggcgcat gcgtgcgggg cgggaccggc 1020 ccggcctata tattgggttg gcgccggcgc cagctgagcc gagcggtagc tggtctggcg 1080 gtgaggagtt gctgcgcgta 1100 // ID HSA_990_1_CDC6 standard; DNA; HUM; 1100 BP. XX AC 990_1; XX DT 06-Sep-2005 (Created) XX DE CDC6: CDC6 cell division cycle 6 homolog (S. cerevisiae) XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.17 35696666..35697765 (FORWARD) CC Score Points: 14 (66.7%) CC Chromosomal Location: 17q21.3 XX CC Database Reference HGNC: 1744; CDC6 CC Database Reference ENTREZGENE: 990 CC Database Reference UNIGENE: Hs.405958 CC Database Reference ENSEMBL: ENSG00000094804 CC Database Reference REFSEQ: NM_001254 CC Database Reference REFSEQ: NP_001245 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:36839_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203968_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203968_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:203967_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203967_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:203968_s_at CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:1536_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:203967_at CC Database Reference TRANSFAC GENE: G001725; cdc6 XX XX FH Key Location/Qualifiers FH FT source 1..1100 FT /chromosome="17" FT /organism="Homo sapiens (human)" FT /note="Genomic Sequence Build: HSA_May2004" FT /note="Genomic Positions: 35696666..35697765" FT /note="Genomic Strand: FORWARD" FT misc_feature 239..>1100 FT /note="ChIP-on-Chip Fragment: HNF4a_panc" FT /note="PubMed:14988562" FT misc_signal 964..971 FT /note="TRANSFAC Site R09600" FT prim_transcript 986..>986 FT /db_xref="dbTSS:FBR03237" FT /note="Number of reported TSSs: 2" FT prim_transcript 991..>991 FT /db_xref="dbTSS:HKR02450" FT prim_transcript 992..>992 FT /db_xref="dbTSS:HCR09341" FT /note="Number of reported TSSs: 2" FT prim_transcript 995..>995 FT /db_xref="dbTSS:HKR08621" FT /note="Number of reported TSSs: 2" FT prim_transcript 996..>996 FT /db_xref="dbTSS:TIR03647" FT /note="Number of reported TSSs: 2" FT prim_transcript 997..>997 FT /db_xref="dbTSS:T7R00721" FT /note="Number of reported TSSs: 2" FT misc_signal 999..1006 FT /note="TRANSFAC Site R09601" FT prim_transcript 1018..>1018 FT /db_xref="dbTSS:OFR09612" FT prim_transcript 1028..>1028 FT /db_xref="ENSEMBL:ENST00000209728" FT prim_transcript 1040..>1040 FT /db_xref="dbTSS:HCR00525" XX SQ Sequence 1100 BP; 280 A; 244 C; 288 G; 288 T; 0 other; ttactgaggg gtaaaagata aatgtttacc atcacctaga attgggttct ggcctctaaa 60 ggaacctgag gcttagatga attattggct ttggaagctg gccttcaaat tactgcgcta 120 atttatattt ttcattaaaa actcagcttg cctcttctat atagctgtct tccctggccc 180 tgaaacccta gtgtttcgcc ataaaagatt ttaaaattaa ggggtcataa ttccctcccc 240 atgatgtgtg gattaatggt aagaagatgc acagaacata atattcttag gttgaacgaa 300 ataaaagtaa agagttggct ctgtttctca cctttgaagc acaaatcaag agatactatg 360 atgaagcata gtttttcttt atataggtgt gtagaacttt accataaaaa tcactagttc 420 agccatcagg agatctggat cctaggctct tcactgtcac caagatgctg tgacctctaa 480 ccttgtatag aagtttgctt tgtactttgc gaggttgagc attagagagg taaggaaagt 540 gcctagcatc atacctggcg cacagaaccc aaaacggtag gtatcatgta gcagttctga 600 aaatctagcc catcaggatg atgcaaatgg gtactttagg cagtgagaag gggaaccaca 660 tcttgacact tccagtcgaa ggaagagtgc gactgcgcgg cagcaaagac tacgcctccc 720 agcgtgcttt gcggcgggcc ggcccgcttt acccagagtc gccctgccgc aatcgcgcgt 780 ctttccaccg aggccccgga tgtagattcc ctcccccgtt cagtggtcgt ggcctcacag 840 cgactctaag acttggggct ctctcattgg ctgtaactct tccactggat tggtagcaaa 900 aaaagaggcg gtgcccaagg cgaaaggctc tgtgactaca gccaatcaga atcgaggccg 960 ggctttggcg ggaggtggga acgctgtggc cattcggatt tggcgcgagc gcggctggag 1020 tttgctgctg ccgctgtgca gtttgttcag gggcttgtgg tggtgagtcc gagaggctgc 1080 gtgtgagaga cgtgagaagg 1100 // ID HSA_9976_CLEC2B standard; DNA; HUM; 1100 BP. XX AC 9976; XX DT 06-Sep-2005 (Created) XX DE CLEC2B: C-type lectin domain family 2, member B XX OS Homo sapiens (human) XX CC Build HSA_May2004: Chr.12 9913377..9914476 (REVERSE) CC Score Points: 2 (66.7%) CC Chromosomal Location: 12p13-p12 XX CC Database Reference HGNC: 2053; CLEC2B CC Database Reference ENTREZGENE: 9976 CC Database Reference UNIGENE: Hs.85201 CC Database Reference ENSEMBL: ENSG00000110852 CC Database Reference REFSEQ: NP_005118 CC Database Reference REFSEQ: NM_005127 CC Database Reference AFFYMETRIX: AFFY_HG_U95Av2:40698_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A:209732_at CC Database Reference AFFYMETRIX: AFFY_HG_U133_PLUS_2:209732_at CC Database Reference AFFYMETRIX: AFFY_HG_U133A_2:209732_at CC Database Reference AFFYMETRIX: AFFY_HG_U95B:44399_at CC Database Reference TRANSFAC GENE: G007296; CLECSF2 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: 9913377..9914476" FT /note="Genomic Strand: REVERSE" FT prim_transcript 752..>752 FT /db_xref="ENSEMBL:ENST00000228438" XX SQ Sequence 1100 BP; 283 A; 207 C; 196 G; 414 T; 0 other; gccaactgta tcattctgct taacaggaat ttctaaaacc agcaaagctc atgtttattg 60 acagtaagtt ggctgctgcc tggcttcagg ggtgaggatg aactgcaaag caacagcggg 120 gaacatttcc ctgtgttgaa aatgttttat atcttaactg ttgtatcttg actgttttcc 180 tttttggaac aaaactaaat ttcactcaac catacttgag taatctctat atttttctat 240 acatgctttt ctaatagttc tttggataca atcttttgtt aacaacaaag gtagaatata 300 ttcatttcct catgaatttt ctgtcttttt tttctgtcca aaaatgaaaa gagcaatttt 360 gttatctgtc ctttccttct gcccagaaat gattaaacct gtatttctta ttctcttcat 420 attttctttg ttttaattcc tttgtactac agtttcttct ctattctcat ttgcttttcc 480 tcttcaagtt tctctctcag aacaaatgca gtgttaatcc cgaagccgct tgcgggacac 540 tggcttcttc tcctcagttt cctccctaat atatttgttg aggggtaata caaaatcact 600 gggaaactga ttagagcaga tttgaagaca aaattgtggc ctggtaactt agcaaaagca 660 taatggtgtc atcttgtatg ctgatgataa cgttctgggc actttgttac tttcgttttc 720 ttttttccct ctgtgtgtct ttgtgtgtgt ttgtgtgtgt gctcacaccc acacgtgtga 780 ctttgcacgc atttgtcttt gagagagaga taatagtttt tgtttttctt tcagtagcca 840 aagtttaaac cattgctttt tctttgattc tatcgctttt aaggtgatct ttcttaacac 900 aggataagaa agcagtaatg tcctaaagaa tgctgttgaa ttaattagta tcagcctctc 960 ctacagttct ggaaggatac gtggttaagt accactcctg gatgaatcag aaaaacagcc 1020 acttgagcaa tttcgtgttc tgtggttcag atgagaatcc cagttgagaa agtaagaaaa 1080 tatgtgttta ttcttcagct 1100 //