Tag | Content |
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EnhancerAtlas ID | HS091-39841 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:179106270-179107870 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr5:179106938-179106949 | CATGAGTCACT | - | 6.14 | HNF4G | MA0484.1 | chr5:179107625-179107640 | GAAGTCCAAAGTCCA | + | 7.07 |
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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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Enhancer Sequence | GAGACAAGAG TCCGGGTGAG CAGCGTGCTT GGTACAGGCC GCCTCTCAAA CCGCGAGGCC 60 GGCGGACATG TCTTAGCCCT GCAGCTACGG CTGCGGCTGT GTCTCACCAG CTGCTGGCCA 120 CCGAGGAGCC CGTCGTTCCA CGCTGCACAG GCAGCAGTCT CACCTAAACC ATCTTCCCCA 180 AAGACCACTG AGGATCAGGC CCTGGGATAC ATATGCAGAT GAAGGACGGG AGGAGGGCCT 240 TGTTCTGAGT TGCAGCTGGA AGGGTGAGGG GTAGGGAATG GTAGCAAGAC AAGTAAGTAG 300 GTACTTAAAG GAGGAGTAGG ACTTTGCCAG GTGGGTTGAG GATGGAAAAT GGAGAACTTC 360 TAGGCAGAGG GAAGAGCCGA GCAGGGCTTT CTTTTTCTTT TTTTTTGAGA CTGAGTCTCG 420 CTGTCGTTGC CCGAGCTGGA GTGCAATTGC GCGATCTTGG CTCACTGCAA CCTCCACCTC 480 CCGGGTTCCA GCAGTTCTCC TGCCTCAGCC TCTTGAGTAG CTGAGATTAC AGGCGCCTGC 540 CATCACCCCC ACCTGATTTT TGTATTTTTA GTGAAGACGG GGTTTCACCA TGTTGGCCAG 600 GCTGGTCTCG AACTCCTGAC CTCAGGTGAT CCACCCAACT CGGCCTCCCA AAGTGCCCGG 660 ATTACAGGCA TGAGTCACTG CGCCTGGCCT TTTTTTTTTT TTTTTTTTTT TTTTTGTATT 720 TTTAGTAGAA ATGGGGTTTC ACCTTATTGG CCAGGCTGGT CTCGAACTCC GGACCTCAGG 780 TGATCTGCCC GCCTCAGCGC CAAAGTGCTG GGATTACAGG TGTGAGCCAC TGTACCCGGC 840 AGGGCAGGAC TTTCATATTT CAGATGTGAA CACGAGCTTG GATAGGATTG GTGCTGGGAA 900 GAGCAGAAGA GGAAGCTGGG AAGGTGGACC AGTGCACTAT GTGAAGGTGC CCTACAGGCA 960 GGCTCGGAAG CTTAGACTTC CTTTTGTGGG TAAGAGGGAA CTGCTGAAGG ATTAGAAAGC 1020 CGGGGTTAGA TCTGGATTCT GAAAGCAATC TGGGAGGATA TCTAGCATAG CCAACAGCAT 1080 TATTGCCCTC ATCATTCAGT CATTTGATAG ACTTGAACTA GCATCTGCTC TGTGCCAGAC 1140 TCTGGTCTTG GGAAGGGGAC CTGAAACAGC CTCTGCCTGC CCTCAAGGTG CTCCTAATCC 1200 AGCTTGGAAG ACAGATGCGT GTATAGACCA CAGTCCAGTG TGTTCACTGA CATCCTGGGG 1260 TGTGTGCCAT GGGCTAGACC TATGCATAGG GCTCAAAGTA TCAGGGATTG TGCACACTAA 1320 ACATGACTTT TATTCCAAAC AAACTGTGCC CTCAGGAAGT CCAAAGTCCA GATAACAGAC 1380 AAGTCCCATT TTGCTCACTT CTCTCTGCAC CCCCCACCCC TGCCCAGTAA GTGCTGATTC 1440 TATTATGTGA AAAAGGGAGC TATGTGTTGT TTCTAATTCC TCTTCTGCCC ATGGGCAGTG 1500 AGAAGAGAAA GAACTAGAGC AGGGTTCCCT CTGTTATGCC TTCGTTAATT CATAATACAC 1560 TTATCCCTCA CATATAGGTG GACAGAGGCT GGATGGTACA 1600
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