Tag | Content |
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EnhancerAtlas ID | HS091-08877 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:119040010-119041830 |
Target genes | Number: 25 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:119041636-119041651 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr11:119041636-119041654 | GAGGTCAGAAGTTCAAGA | + | 6.88 | TEAD1 | MA0090.2 | chr11:119040330-119040340 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr11:119041080-119041101 | AAAGGAGCAAGGGAAGAAAGA | + | 6.29 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I119170 | chr11 | 119041021 | 119041067 |
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Enhancer Sequence | TGTACGTTTC CTGCAGTGCC CCCTCCTTTT CTCATTGCCC TGGAGACCTG GGTGATCACC 60 GGAGAACTGC CCTCGGCCCC GCAAGTCCCG TCTTGACTCA GTGGCCCTAG ATCCGAGGTT 120 AAACCGGAAC CTAGGCTTTC TCAGGCTTCT GGAGCCCTCT CTTAACCCTT CCGCAGCCCC 180 TGGGACGGGC CAGCACCCAG CCAGCTCCTC CGCTGGTTGG CCCTGCTAAG GCAGGTGGCC 240 CAATGCAGCC AGTTCTCCTT AAGCGTACCC TGCCCAAGAA GCCCCGATCT CAGTGGAGGA 300 GACCAGGTGC CAAATAGGGG CACATTCCAT TTAAGTGAGT TCAGAGGCCT CAGAAAAGAC 360 TTCCCAGGGA CGGAGACTTT TGAGCAGGAT CTTAAAAGAT TGGTTGGGGC CCGAGTGGTG 420 GCTCGCGCCT GCAGTCCCCG CACTTTGGGA GGGCAAGGCG GGCGGATCAC TTGAGCCCAG 480 GAGTTCGAGA CCACCCTGGG CAACAATGGT GAAAACCCCG TCTCTACAAA AACCAAAGCC 540 AAAAATTAGC CAGGTGTGGT GGCACACCAC TTTAGTCCTA GCTACTCAGG AGGCTGAAGC 600 AGGAGGATGG CTTGAGCCCA GGAGGTAGAG GTTGCTGTGA GCTGAGATCG TACTACTGCA 660 CTCCAGCCTG GGCAACAGAG CGAGAGACCC TGTCTCAGGA AAAAAAAAAA AAAAAAAAAA 720 AAAAAAAAAA AAATTGGTTG GGACTCTAAC AGAGGAAAAA GGTCATTCCA AACTGGGAAG 780 AGTGTATGAA CAAATTTAGG ACAGCAAGAG CAAGAATCCG GTGAGCCTGG GGTATAAGGC 840 ACAGGCTGGG ACAAACTCAG AAAAATAGCT TGTGGGAGCC CAGTGTTTGG ACTCTATAAG 900 TAACCTTGGA CTTTTCGGGA GGTGCTTGGT GCTTGGGGTG AGGGATTAGA ATGGGATGAG 960 ACTGAAGGCA GAAAGGCTGG TGAGGAGATC GGGTCCAATA AATGCTGGTC GGGGCAGCAA 1020 CTGGCTGGCA AAGCAGTGGG GAGGAATTGC TAGGACTCTT CACACTGCCT AAAGGAGCAA 1080 GGGAAGAAAG ATTTGAAGAG AGAGGTCAGG TTTCTAATGT AAGGCGTGGG TGGGAAGATT 1140 TGCAGCAAGG TAAATGACAA GAGGAGGGGA ATGATGAGTT CAGTTTTACA TGGGAGAAGT 1200 TTGAAGCAGT GGCAGGTTGT CCATCTGGAG ATGTCAAGTG AGAAGTTCAT TCATTTATTT 1260 ATTATTTATG TCAGCCTCAA AGGCTGCTTA CATAAAAGTC ACAGAGAACA TAAAATGATG 1320 AAGCCATTAA AACTCAGCTA AAAGGATCTG ATATCTGCGG AAGAAAGGCA GAGTGGGGTG 1380 GATAATTATT ACTGGAAAAT CTAGGCACAG AAAAGCCACT GAAAATGAAC ACAGGACTCC 1440 TATCTGAGCT TGCTGGTGGC CAAGAAGGAA AAAGGACACC TAAATAAAGC AGTTTACCAG 1500 GGTGGAACTC AGGGAAAGGT GTTCGTGAAG CTTCAGGGGA GAGGCAAGAC GTGGCAGGAA 1560 GGCCAGGTGT GATGGCTCAC ACTTGTAATC CCAGCACTTT GCAAGGCCAA GGCAGGCAGA 1620 TTACCTGAGG TCAGAAGTTC AAGACCAGCT TAACCAACAT GGTAAACCCC GTCTCTACTA 1680 AAAATACAAA AATTAGCCCA GTGTGGTGGT GGGCGCCTGT AATCCCAGCT ACTTGGGAGG 1740 CTGAGGCAGG AGAATCGCTT GGGCCCGGGA GGCATAGGCT TCAATGAGCC ACAATCATGC 1800 CTGGGCAACA GAGGGGCACT 1820
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