Tag | Content |
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EnhancerAtlas ID | HS116-09169 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:123882760-123884110 |
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: 2 | Chromosome | Start | End |
chr12 | 123882766 | 123883905 | chr12 | 123883000 | 123883784 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I123397 | chr12 | 123882456 | 123884323 |
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Enhancer Sequence | GGTAGTTGCA GTGAGCCGAG ATCGCGCCAC CGCACTCCAT CTTGGGTGGC TGAGCAAGAC 60 TCCGTCTCAA AAAAAAAAAA AGACAGCACT GCAGATGGTG AGGTGGTGCC AGACCACAGA 120 ATCCCAGACA CCTCCCAGCC AGGGTTGGAG CTGCGGTGTG CCCACACACA GGGCCTCTGC 180 TGAGCGTCCA CCAAGGGCTG CTGTGGACTT TAGGGTGGGG GGAGCCGAGT TGGCCTTGTT 240 AATAAGAAGC AAGAGTTTGT GCTGGGCAGA GTGAAGGCTG CGATGGGACA GGATGCAGGT 300 CTGCTAAATC TTGCAGCAGA TGAGCAGAAG GGAAGAACAC ACTTGCTTCC CTAAAGCACA 360 GTCTGCAAAC ACAAGAAAGC TCGCCCTGTT CCTGGACCGG GAGCCGTGCT TTGCCCCCCA 420 CTGTTTGTGT TGGCTCTGCT GAGTGCAGCC ATGCAAGCTG TTGCTGGCCA GGGCAGGGAG 480 GCCATAGCTG GCCGGGATGA CGTGGCTAGA GCTGGTCAGG GTGGAATATT TTCTGACTGC 540 ACAGATAAAG CCCAAGAACG GGACAGCTGG GGCTCATCTG AAGGGTGGGG TCAGTCCTGA 600 CTTGACTGCC ATGCTGGGCC CAGGCTGTGG ATCCAGGAGG GTGGGGCATA ATACAGCCTG 660 TTGTTGGCCA GATGGTCTGG GGTGAAACTG CAATTCAGAG CCTCTTATAT ACCTCCACTG 720 AGGCTGAAGA CAGCAGCCAG GGCGGGCCTA GCGCCAGGGC GTGGGTCCTG GGCAACAGGG 780 TGGGATCAGG GCTGCTGGAT TTGGACACAA GGTGGGCCTT GGAGAGATGC CCTATCCACC 840 AAGTGCTTCA CTGCAGGGGC CCCTTGGCCG GCCAGCCTGG CTGTGGGTGG GGTGGCAGCC 900 AGCAGCGGGG CAGGGACCAT GCCTCTTGGC AATGGCTGGG CTTCCTCATG CCCAGCTCGG 960 CCCCAGGGCC AGATGTGCAA GCAGCCTGCT GATTCCGCTT GGGAAGGTCC CCTCCTTCCT 1020 GGTCACAGGC GCTTCTCAAC TGCCCTAGTT CCAACCTTGT ATCCCTCCCA CTCCATCTCC 1080 TTCTAGGCCC ATTTGTGGGT TCCTGCCAGA AGTCCCTTTA GAAAACCCAG GGCTGGTTGT 1140 TTGCAGGCCC CAAATTCCAG GCCTTTGGGA GACTCAGCCT CCCTGGCTTT GTGCCGGGGC 1200 ATCTGGCCTG GTCCCAGCTT CCCTCTGCGC ATCTCCTACC TGCCGTGTTT GGTCCCAGCA 1260 GAAAAACCCC CATTCCACTA CCCCGGTCTT TCCATGATCA CTCCCGTTTA CATGGGCCCC 1320 CGTACTTCTC AGCACTCTCT GCACACTTGC 1350
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