Tag | Content |
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EnhancerAtlas ID | HS118-03498 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr11:61342960-61344190 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr11:61343248-61343259 | TGCTGTTTACA | + | 6.14 | KLF4 | MA0039.3 | chr11:61343100-61343111 | GGAGGGTGTGG | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCCCACACC GTCATGGAAA TGCTTGTATC TTACACATGA AAGCTCCCAT GATCACCCCC 60 GTCCACACCC ATGTATGCCA CACAGCCAGG TAAGGCCCTG CTCCGAGCAG ACGAGGCCTT 120 CATGGCCATG CCAGCAGGTG GGAGGGTGTG GCAGGGGGTA GGCAGGGTCC CTGGCACACA 180 GGCCCTGCCT GGCCAGGTAC AGGGCCGGGG GAGGGGCCCT CCCCTAAAGC TTTCCGTCAT 240 AGCTCCCCAC GCACCTCAAC GCGCCTCGCT ACAAATACAC TCATTAGCTG CTGTTTACAG 300 CGGTCCTGGC ACTTCGATAA GCACAGATAT TATGGCCATC CAGCTGCCAC CCGCACACAC 360 ACTAGGTACA CATACAGACA GTGCCTCTCC CCCTGCCTCC GCCCTCCCCT TCCACCCGTG 420 GGCTCAATCA CATGAAGATA CCAATTCCCC AAACATGCAG CTTTGCAGGG GTTCCAGCTC 480 ACAATACCTC AGCTCCCGGT CCATTCTATC CCAAGGGGTC CTTCCAGGTG GAGGCTGCAG 540 AGACTCCCCA GAGCAGGCCG GATGCACCTG CCCGCCTTCC AACCAACTGG ACCTGGAATT 600 CCAGGCCAAA GCTCTGGGCA CAGTCCAGCC CTTTCCACAA GTCCCATGCT GTCTGCCAAC 660 TCTGTTCCAG CCCTTGGGGA ATTCTGCTGG GTGAGACCAA AGCCCTGCCC TGCAGACACT 720 AGTTGGACAG GGCCCAGCAG GGCTGCCCCT GCTGCCTGGA AGGTCAGGGA CCTCCATGCC 780 CACGGAACTG GCAGAATTCA CCTGGCATCA CCAGCTGGGG TTCCCTGGCA AGGCAGGCAG 840 GCACCCGGGC TGGGCCTGGC ACAGGCTGGT GCCGGCACCT GGCCAGACCA GTGACTGCCC 900 CGACGAGAGA AAGTTGACCT CTCGGCCACA TATGCCACCT GCCGGGCACT GTCTGTGGAG 960 CAGAGGACCA GCTCTATACA GGGCTGCCCA TGCCCACCTG TGATGCCACA GTGCTCTGAG 1020 GAGCCATCAA GCCAACTCAT TCTCCAGCTG GGGGTCATCA GCTCCGGACT GGGCCTCCCG 1080 CCCCCACGTG ACCCCTCCCA GCTCTTCTCC CTGCTGTTCT TCTGTTCTTG GCCTCACTCC 1140 CCTGGGGGAA CCAGTTATTG AAAACGAAAA CGGTCCATCA GATTCAATAA GGATTCAAAG 1200 TCCGTGAGAG AATAGGGGGT GGGTGGGGAG 1230
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