Tag | Content |
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EnhancerAtlas ID | HS050-17602 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:123882620-123884210 |
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: 3 | Chromosome | Start | End |
chr12 | 123882766 | 123883905 | chr12 | 123883000 | 123883784 | chr12 | 123884027 | 123884111 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I123397 | chr12 | 123882456 | 123884323 |
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Enhancer Sequence | GGAGTTCGAG ACCAGCCTGG CCAACATGGT GAAACCTTGT CTCTACTAAA ATACAAAAAT 60 TAGCCAGGCA TGATGGCAGG TGCCTGTAAT CCCAGCTACT TGGGAGGCTG AGATGGGAGA 120 ATCACTTGAA CCCAGGAGAC GGTAGTTGCA GTGAGCCGAG ATCGCGCCAC CGCACTCCAT 180 CTTGGGTGGC TGAGCAAGAC TCCGTCTCAA AAAAAAAAAA AGACAGCACT GCAGATGGTG 240 AGGTGGTGCC AGACCACAGA ATCCCAGACA CCTCCCAGCC AGGGTTGGAG CTGCGGTGTG 300 CCCACACACA GGGCCTCTGC TGAGCGTCCA CCAAGGGCTG CTGTGGACTT TAGGGTGGGG 360 GGAGCCGAGT TGGCCTTGTT AATAAGAAGC AAGAGTTTGT GCTGGGCAGA GTGAAGGCTG 420 CGATGGGACA GGATGCAGGT CTGCTAAATC TTGCAGCAGA TGAGCAGAAG GGAAGAACAC 480 ACTTGCTTCC CTAAAGCACA GTCTGCAAAC ACAAGAAAGC TCGCCCTGTT CCTGGACCGG 540 GAGCCGTGCT TTGCCCCCCA CTGTTTGTGT TGGCTCTGCT GAGTGCAGCC ATGCAAGCTG 600 TTGCTGGCCA GGGCAGGGAG GCCATAGCTG GCCGGGATGA CGTGGCTAGA GCTGGTCAGG 660 GTGGAATATT TTCTGACTGC ACAGATAAAG CCCAAGAACG GGACAGCTGG GGCTCATCTG 720 AAGGGTGGGG TCAGTCCTGA CTTGACTGCC ATGCTGGGCC CAGGCTGTGG ATCCAGGAGG 780 GTGGGGCATA ATACAGCCTG TTGTTGGCCA GATGGTCTGG GGTGAAACTG CAATTCAGAG 840 CCTCTTATAT ACCTCCACTG AGGCTGAAGA CAGCAGCCAG GGCGGGCCTA GCGCCAGGGC 900 GTGGGTCCTG GGCAACAGGG TGGGATCAGG GCTGCTGGAT TTGGACACAA GGTGGGCCTT 960 GGAGAGATGC CCTATCCACC AAGTGCTTCA CTGCAGGGGC CCCTTGGCCG GCCAGCCTGG 1020 CTGTGGGTGG GGTGGCAGCC AGCAGCGGGG CAGGGACCAT GCCTCTTGGC AATGGCTGGG 1080 CTTCCTCATG CCCAGCTCGG CCCCAGGGCC AGATGTGCAA GCAGCCTGCT GATTCCGCTT 1140 GGGAAGGTCC CCTCCTTCCT GGTCACAGGC GCTTCTCAAC TGCCCTAGTT CCAACCTTGT 1200 ATCCCTCCCA CTCCATCTCC TTCTAGGCCC ATTTGTGGGT TCCTGCCAGA AGTCCCTTTA 1260 GAAAACCCAG GGCTGGTTGT TTGCAGGCCC CAAATTCCAG GCCTTTGGGA GACTCAGCCT 1320 CCCTGGCTTT GTGCCGGGGC ATCTGGCCTG GTCCCAGCTT CCCTCTGCGC ATCTCCTACC 1380 TGCCGTGTTT GGTCCCAGCA GAAAAACCCC CATTCCACTA CCCCGGTCTT TCCATGATCA 1440 CTCCCGTTTA CATGGGCCCC CGTACTTCTC AGCACTCTCT GCACACTTGC AATGAATGGG 1500 TCACACAGCA AGGTGGTTAT GTGTGTGATG GTGGTGGTGT TGCTTTGAGG GCCTGCTGTG 1560 TGCACTGTTC TAGACCAGGA GATTCCACAG 1590
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