Tag | Content |
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EnhancerAtlas ID | HS118-17566 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr7:101877520-101878740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:101877983-101877998 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAAGTCTCC CTGCCCCGCC CGGGCCGGCT GCGTCCGCAT TCATAGACAG GCTGTTTCTT 60 TCAAATCTTT CACACACAGC TGATGAGGGA CATTGACCCA TGACCAAGGG ACCAGAGGAC 120 AGGGCAAAAA TATTTTTGGA TGGTCATCAG CTAATGAGTA CCTAAGAGGG CTGGAAAGTT 180 GTGTAACTTT TTCTCTCCAG CAGCCTGAAT CTAAAGATTT TTTTAGCACT GGGAGCACTT 240 TTAACCAAGG AGAGCGAAAC AGCTCTGGGG GCGCTGCATT TGGTTTTTGT GTTGTGTGGG 300 TGGCTGATCG GGCTATCACA GCATTTACTG AGCATGTACC AGGTGGCTAG AGGCCTTCCT 360 TTGTTATCAG AGAGAGAAAT AAGAAATGCA TTTTGTAGGC AGGGCACGGC GGCTCACGCC 420 TGTAATCTCA GCACTTTGGG AGGCTGAGGC AGGCGGATCA CTTGAGGTCA GGAGTTCAAG 480 ACCAGCCTGG CCAACATGGC AAAACCCCCT CACTACTAAA AAAAAAAAAA AAAAAAAAAT 540 ATAGCCAAGC TTGGTGGCGT GCGCCTCTAT AATCCCAACT ACTTGGGAGG CTGAGGCACA 600 AGAATCGCTT GAACCCTGCA GGCGGTGAAC AGAGATTGAG CCACCGCACT CCAGCCTGGG 660 TGACAGACCA TGACCCTATC TCAAAAAAAA AAAATGCATT TTGTAGATCA GGAAACAGAG 720 GTTCAGAGAG GTTCGGTGCC TCCACCAAGG TCACCCGGCC TGGAAAGTGA CAAAGCAAAC 780 TCCTGCCACA ACAGATCTCT CTCTTGCTGT TATTTCCCAG CCTCTGGGGA TTTGGCCTCC 840 CTAGAGGAAT AACCCCACGT GCACCCACAT GTCATCTCGA ATGTGGATTC ATGTTCTTCT 900 TGCAGCCTGT AGGCTACAGC ATAGGAAAAA TGCCTAAAGC CAGGTGTGCT GTGCCTCTTG 960 GTTTGCAGTT TCTAAGCGCT GGTCCTCGCC AGTGAGTCCG CCCCTCGAGC ACCCTCAGTC 1020 CTCAGGTCAC CTATGGTGCT GGGAGCTCAC TGGGCGGCTG AACTGCATCC CTTAGGGGCA 1080 GAGACTGGGA ACCAGCTGCT GCCGGTCTGA CCGTAAGAAG CGGCAGCCTC CCTGATCAGC 1140 TAACGCAGAG GACCTTAACT AAGAGTGGGC ATCCCAGGGG CCGGGCACAG TGGCTCATGT 1200 CTGTAATCCC AGCACTTTGG 1220
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