Tag | Content |
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EnhancerAtlas ID | HS195-01668 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr12:110260350-110261690 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I109822 | chr12 | 110260249 | 110261532 |
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Enhancer Sequence | GGCATTGCCT TGCTCCAGAA AGGGGGAGGC AGGATTAGAA CCCATGCATC CCCGGGACCT 60 GCGCCTTTGA TGGACACTTT ACAAAGACAA GGGAACTCTG GGAGGGAGAA GCTGGAGAAA 120 GAATGGAGTG GGGGATGGGT CGCAGTCCCT GACGAACCAC CAGTTCACCA GCTCTGGGCA 180 AGTCACCTGG CCTGCCCATG CCTCGGTTTC CTCACCTGAA AAATGGCAAT GATCCTAGCA 240 CCTACCCCAA GGGAACTGTC GTGAGGGTTA CATGAGATAA AGCATGCAAA ACACTGAGCC 300 CAGTGCCTGG TACAGAGCAT GCATTCAGTC AAGCATGGCT GCTGTTGGAA TCATCAGTAT 360 CAGTGTACTA TTTATTAGTA TCATTAGGGG AACAGATGAA CAAAAGGACT GAGGACCAAG 420 GAAGGCAATG ACTCCTAGAG AAGGCAGAGC GGCCAGATCC AGAGCCTTGG AGGTAGACTC 480 TGGCAGCCAC CTCGAAGTGG CGGCTGCTGG GAACAGCCGG CTGGGAGCTC AACTCCTTGG 540 CCAGGCGAAA CCTACTGCCT GCCAGGCTAC CCCACGGCTC CCAGGCACTT GGCAGGCGGC 600 AGCAGTAGGG GGGCATCATG CCATGCCCAG CACCTTCCCT GGCCAGCCTG TATTTACCTA 660 GCAGGTCTCG GCCCAGCCCG CTTCCTGTTT GCTGCACAGT GGCCGCCTGT CCAGGACAGA 720 CAGAGCCCCA GTGTCCTGCT GGGCCCCCAC CCCATGCACT CACACCACCC AGGCAGGGCA 780 GGTCTGGGGT GACTCACCGC GCCCCACGGA GGGCAAGGCC AGCGTGGCCA CGGCAGTCAT 840 TTGGTCATTC TGCAAGCCCT TGGCTGGAGG GAGGCCGGCT GACAGCACAC ACAGATGCCC 900 CTCTGAGCTT TCACAGGGAC CAAGTCATTT CCAAGGGTCC CGGCCCCTGG GTAGGAGCCA 960 CCAAGAAGCG GTGTGGCTTA ATGGTTAAGA GCATGCACCT TGTAGACACA AAAGGCCACA 1020 TATTGCAGGA TTCCATTTAT ATGAAATGCC CAGAACAGGC AAATCCACAG AGACAGAAAG 1080 CAGATTAGTT GTTGCCAGGG GCTGGGAGTG GGGAGTGGTG ACTGCTAATG GGTACAGAGT 1140 CCTTTTTTGG GGTGATGAAA ATGTTCTGGA ATGAGATAGT GCTGATGTCT GTACAACTCT 1200 GAATACACTA AGAAACCAAC TGAATTGTAC GTTTTAAAAG ACTGAGTTAT GAGTATGTGA 1260 ATTACATCTA AATGACCCTT CCAGGCTTAG TGACCTCAGG CAGGTCACTT CCCTCCCAGA 1320 ACCTCAGTTT CCTTGTTGCA 1340
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