Tag | Content |
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EnhancerAtlas ID | HS118-07780 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr17:8373210-8374700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:8373244-8373259 | TGAACTCTTGACCTC | - | 7.64 | RARA | MA0729.1 | chr17:8373241-8373259 | TCTTGAACTCTTGACCTC | - | 6.45 | Zfx | MA0146.2 | chr17:8373269-8373283 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01584 | chr17:8372303-8377640 | Aorta |
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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 |
GH17I008469 | chr17 | 8372402 | 8374500 |
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Enhancer Sequence | AGGCAGGGTT TCACCATGTT GTTCAGGCTG GTCTTGAACT CTTGACCTCA GGTAATCCAC 60 CCGCCTCGGC CTCCCAAAGT TCTGGGATTA CAGGTGTGGG CCACCGTGGC TGGCCTTAGT 120 GACGTTTTTT TTGTGGCTCT AGCAGCTCTT GGCAAATGAT CCCCCGTGAA GAAAGCAGCC 180 AACTCCCTGG CTCATCTCCC GCTTTCTGTT TGGACTGTGG GGTGTAAGAT GCTACTTTGG 240 ACATGGTCAG AGAGAGCATC TGCCACCTGG CATGAATGCC GCTACGTACC GTTTGCCTGT 300 CTAGCTGAAG AGTGCCTCTG GGTAGAGTGC CTCTGTGTGG GTTTTCTTCC TGGAGCTGCC 360 GGGTACCTGG TTTTGCATGG CTCTCCATGA AACCTCGGGA ATGAGCCTTC CTTGAGCCGC 420 ATCTGTGTGC CGTTCCTCCC TGCTGGTGGG GCTGATCTCC CGGGTGGTGG ACAGCTTCTT 480 GCCTCCAGGT GTTTTCATTT CAGCCGCTCA GTCCTATCCC TTGCTCCCAA ATATTGTCTT 540 ACAAGAGAGT AGTAGCCAGC GCTCCACTTC CTTCAGCCCA GAGTGGCCAG AAATGATCCC 600 TGACCAACGC AGCTGAGACC CAGGAGCCAA AGCTGGGACC TTGAGTCACA GTGAGGCCTG 660 CAAGAACTAT ACAGAGGTGA CCTGAGGACA GGACACAGTG CTCTGACCTC AGGTGGCAGA 720 AAGGACAATG GGCCCGGGTT TGAGTTGACT GAGCTTGCAC GGCTAATTCA TGGTGAAGCC 780 AGGCTTGGGC ACGAGCCCAG TCTTTTTCTG CTGTGCCTTT CCAGACTTGA GGCCTCACTG 840 GCCTTGACTC CCACGCTCTG TCCTGTGCCT TGGGAGAGGA GCAGGTTTTG AAGGCTTGGA 900 AATGACGAGC GGCGGGGCCG GCACAGCCTT TGTAGCAGGA GGAATCGGTT CACGTAGCCT 960 TCCTCCTGTG CCCGCTGCGC ATGCTGACTC CGCCTTTCTT GGCAGCTGCC CCGGAGATGC 1020 CACTAGTGCG CATCTCCTGA GAGCCAAGGT GGAAGCTGGC ACTTCTGGGA GAGGGGAGGC 1080 ATCCTGGGTG GAGCCACGGC TTTAGGGAGC ACCCGGTAGC CAGCTCTGCC CCCTCCCCGA 1140 CTGTAACAGT GTTGTGCCTT GTCTCGTGTG TTGGTGATAC AGCATTCCTG AAAAGCAGAT 1200 TCCAGTGAGG CTCCACAATT TCCTTCTAAG CTGCTGATGC TCATTCTGCA AGTTTTTTGT 1260 TGTTGTTGTT TTTTTGAGAC AGATTTTCGC TCTTGTTGCC CAGGCTGGAG TGCAATGGCG 1320 TGATCTTGGC TCACTGCAAG CTCTGCCTCC GAGGTTCAAG CGATTCTCCT GCCTCAGCCT 1380 CCCAAGTAGC TGGGATTACA GGCATGTGCC GCCATGCCCG GCTAATTTTG TATTTCCCAT 1440 TCTGTAAATT TTGATGCTGT GCTTTATCGA TCTTTCCAGG AGTCGGGCAA 1490
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