Tag | Content |
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EnhancerAtlas ID | HS118-17210 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:47754870-47756160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr7:47755542-47755553 | TGTAAACAAGA | - | 6.02 | IRF1 | MA0050.2 | chr7:47755031-47755052 | GCATAGTTTCTCTTTCAGGTT | + | 6.16 | Nr2f6(var.2) | MA0728.1 | chr7:47756042-47756057 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58755 | chr7:47740634-47784121 | Ly1 |
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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 |
GH07I047715 | chr7 | 47755164 | 47755427 |
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Enhancer Sequence | TGTAGGAAAT ATTGAATAAA TCCTCATAAA ACAGCAGCAA TAACCATCAA AACTTTCTCG 60 GCAATTTGAG GAAGTTCCAT TGGGTGCTGA AAACACAACT GTCCTTTGAA CACAAGGATT 120 GACTGTGGGG GAGATGCTGT GGTCTTGGAT GGTTGTCATT TGCATAGTTT CTCTTTCAGG 180 TTTCTTTCCT TCCAGCCATG CAGACCAACA TCCAATATGA TCACAGCAGA TGCAATCTCA 240 GTCTTTACTT AAAGTAAGCT TCCTTTGCTA CAGAAAGGCC TAATCTTTTC CATTCATTTT 300 TTGTGGACCA CCACAGTGCG ACACCCCCAC CCCAACCCAA GTAGGCACAT GACAATTGTG 360 AAGTAACCAG AGGTCATTGG TTGTGACCCG CGGGTAGCCA TTTTGACCCA TGAAGGCCCT 420 GCGTGGGGCA GGGCAGGTTA CATGTCAACA TATACTTCTG GAAAGTGCTT GATCATATGT 480 TCAACTAAGA AACCATTGGC ACCTCCTCTC ATCCCATGCC TAAGTCCTTT CCTCAGCATG 540 CTCTGTTAGG GAGACCCCAC CTATTTTGTC TCTGCCTAAC AATCATACAT GGGGGCCTAA 600 TGTCCCTGGT GTTACAGATT AATGTACAAC ATTGTCACCC CTGCTAAAGA AGGACTCGCT 660 GGGCTTCCCA TCTGTAAACA AGAAGGCAGG GCTTGCATGC ATGAAACACA AGGACCCTGG 720 ACTTGGTGCA AAGGGCTCTG ACTTGGTGCC CGGCTCTCCA GCTGGATCTA GGCCTGTCCT 780 TTAATTTTCA TGTCTCAGAT GTCTAACCCG AAAAAGGGGA GAGAATTCCA ATCATTACTC 840 TGTGTGGAAA AAGTAAAGCG TCTCTTTTTT GATGGGATCT TTATCCATTA ATAATTTAGT 900 TGGACTAAAT TATTTACATT TAACTTGTTA AAGGTCTATT TATTTATATA TTTTTAAATT 960 TTTATTTATT TATTTTTTTG AGATGGAGTT TCTCTCTTGC TGGAGTGCAA TGGTGCGATC 1020 TGGGCTCACT GCAACCTCTG CCTCCCGAGT TCAAACGATT CTCCTGCCTC AGCCTCATAA 1080 GTAACTGGGA TTACAGGCAC CTGACACGAA GTCCGGCTAA TTTTTGTATT TTTAGTAGAG 1140 CCGGGGTTTC GCCATGTTGG CCAGGCTGGT CTTGAACTCC TGACCTCAGA TGATCTGCCT 1200 GCCTCGGCCT CCCAAAGTGC TGGGATTACA GACGTGAGCC ACCGCTCCTG GCCCTATTTA 1260 TTTTTTTAAC CTAATGACCT AATAGCACTT 1290
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