Tag | Content |
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EnhancerAtlas ID | HS118-14812 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr5:32458640-32459510 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF8 | MA0652.1 | chr5:32459471-32459485 | AGTTTCAGTTTCAG | - | 6.86 | OLIG2 | MA0678.1 | chr5:32459411-32459421 | ACCATATGGT | + | 6.02 | OLIG2 | MA0678.1 | chr5:32459411-32459421 | ACCATATGGT | - | 6.02 | STAT3 | MA0144.2 | chr5:32459382-32459393 | CTTCCCAGAAA | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCTGAAATG ATCTCCTTTG GCTTCATGTC TCACATCCAG GACACCCTGA TGCAAGGGGT 60 AGGCTCCCAA AGTCTTGGGC AGCTCTGCAG GGTATAGCCC CTGTGGCTGC TTTCATGGGC 120 TGGCATTGTG TGCCTGCAGC TTTTCCAGGT GTACAGTGCA AGCTTTGGTG GATCTACCAT 180 TCTGGGGTCT GCAGGATGGT AGCTCTCTCC TCACAGCTCC AGTAGGCAGT GCCCCAGTGG 240 GGACTTTATG TGGGGGCTCC AATCCCACAT TTTCCCTCTG CATTGCCCTA GTAGAGGTCC 300 TCCATGAAGG CTTCACCCCT GCAGCAGACG TCTGCCTGGA CATCCAGACA TTTCCATAAA 360 TCCTCTGAAA TGTAGGCAGC GGCTGCCAAG CCTCAGCTCT TGATTTCTGC AGGCCCGCAG 420 GCCCAATACC ATGTGGAAGC TGCCAAGGCT TGGAGCTTGT ACCCTCTGAA GCAATAGCCC 480 AAGCTGTACC TTGATCCCTT TTAGCCACAG CTAGAGCTGG AGCAGCTAGG ACACAGGGCA 540 CCAAGTCCTG AGTCTGCACA GAGCAGCGGG ACCAAGCTCT GGCCCAAGAA ACCATTTTTC 600 CCTCCTAAGC TTCCAGGCAT GTGATGGGAG GGGCTGTTAT GAAGGTCTCT GACATGCCCT 660 GGAGACATTT TTTCCCATTG TCTTGGCTAT TAACATTCAG CTCCTCCTTG CTTATGCAAA 720 TTTCTGCAGC CGGCTTGAAT TTCTTCCCAG AAAAATGGGT TTTTCTTTTC TACCATATGG 780 TCATGCTGCA AATTTTCCAA ACATTTATGC TCTGCTTCCC TTTTAAACAT AAGTTTCAGT 840 TTCAGATAAA CTCTTTGTGA ACACACACGA 870
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