Tag | Content |
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EnhancerAtlas ID | HS118-04043 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr11:128767770-128769100 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:128768879-128768900 | TATTTCTTTCACTTTGTTTTT | + | 6.58 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 128768768 | 128768938 | chr11 | 128768939 | 128769098 |
| Enhancer Sequence | TGCTCCGGCA CCATTTGTTG TAAAGGCTGT CTTTCCTCCA CTGAATTCCT TTTGCACTTT 60 TGTCAAAAAT AAGTTGGGCA TATTTGCAAA GGTCTATTTT TGGGTTCTCT GTTCTGTTCC 120 ATCAATCTAT GTGTCTATCC TTCTGCCAAT ACCACATAGT CTGGAGTTTC CTCATAACTG 180 CAGTTATGTA ATGAGTCTTG AACTTGTGTA GACTGATTCC TTCCACTTTA TTCTTTTCCA 240 AAATTGTTTT ATCTATTCTA GTTGCTTTCC CTTTTCACAT AAGTTTTAGA ATAATTTTAT 300 CTATATCTAT AAAAAATCTT GTGAGATTTT GATAGAAATT GCATTGAATC TGTATATGAA 360 TTCAGAGAGA ATCAACGTTT TTACTATATT GAGTCTTCCA ATCCATGAAT ACAGTATGTT 420 TCTCCATTTA TTTGCTATTC TTCAGTTTCT TTCTTTGGCA TTTTGTAATT GTCAGCAGTT 480 CTTTTTGCTC TGCCATGAAC TAATTGTGTC GCCTTGGACA TTAGTCTTTC AGACCTTCAG 540 TTCTCTTTCT GTAAAATGTG TCTAATAACA CCTACCTTGA AATGCCATGG GAAAGTCAAA 600 TAAGTTAGCG CATGAGCAGT GCCCCATGGC AAGCGCCAAG ATGCAGTTCC CTTCAGCTGG 660 GTCTCTCATC TGTTCTTTGT TTCCTCCTCC TCAGCTTTCG TTCTAATGCC CACATCCACT 720 TACACTTCAC TTTGTCTTTC CTTTTTGTCC TTTGCTTTTT TAAATCCTTC TTTCATTCTC 780 AACTCCTTAC TCTGATTTTT CTATTTCTTT CTTTCTTTCT TTTTTTTAGA CAGAGTCTCA 840 CTCTGTCACC CAGGCTGGAG TTCAGTGGCG CAATCTCGGC TCACTGCCAA CCTCTGCTGT 900 CTGCGATTCT CATACCTTAG CCTCCCGAAT AGCTGGGACT ACAGGAACTC ACCACCACGC 960 CCAGCTCATT TTTTTTGTAT TTTTAGTAGA GATGGAGTTT CACCATGTTC GCTACGCTGT 1020 TCTCGAACTC CTGACCCCAG GTAATCCGCC TGCCTTGGCC TCCCACAGTT CTGGGATTAC 1080 AGGCGTGAGC CGCCGTGCCT GGCCTTTCCT ATTTCTTTCA CTTTGTTTTT CTCTTATTCT 1140 CAATGGATTT TTCTGTTTCA TTTCTTACCC CATGATATTT GTCTATCTCC TCTTTCTTGA 1200 ATCATTTAAG CATTCCATTT TTGTGGAGTT GCTCAGACAC TGAGTGTGAG TCAAGGGCCA 1260 CTCAGCCTGG GTTCAACTCC AGATCAACCA CTTACTAGAT TTGGGGCAGT TGACTCACCC 1320 TCCTGCACCT 1330
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