Tag | Content |
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EnhancerAtlas ID | HS091-06505 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr10:118441390-118442560 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:118442012-118442031 | CGGCCACAAGGTGGCGCGT | + | 6.2 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I116682 | chr10 | 118441941 | 118442130 |
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Enhancer Sequence | AGTGGCCGAC AGAAAGAAAA TGATGACGGG TAAGAAAGCA TGAAAAAGCA GAGATCATTT 60 GCAGTCAGTG AAGGCAATAG CATGAGGAGA TTTAGGGATG GAACATTAGT GACATTTGAC 120 CAAAATAAGT CAATACGATG TCGGGAATCA CAAAGCCAGC TCTTCCCAGA GAAAGTGATT 180 TCCACCGGCC TTCCTCTATT CCTCGGCTTA GCCTGTGCCC AGCTGAAAAG CCCACCCTGA 240 TGAGATTCTC ACAACAACCC TTGGAATTAG GTGGAATTAT TATCCCCATT TTCCACGTGA 300 AAAAAACTGA AAGAAGAGAA TGTGGTCAAA TGTGCGCCAC TGCACTCCAA CTTGGGTGAC 360 AGAGCGAGAC TCTCAAATGA GACCTACCCT GGTCACATTT TTTGGAGAAT GGGTTAATGA 420 AATCGCCTAG TTTCCCGGCT TTGCTGCCCC AGGGAGGAAG CTATCTGCCA AACAGCCTGC 480 AGTGCGCTCA GTTAAACAAT TCCAAATCAA GGAATTTTGT CTGATACAAG GAATTTGGGG 540 TGTGTTTTCC TAACATGCAC CCTGGGTAAA TAGACTGGGG GGGGGGGCCA TTTCCTGACC 600 CAGCTGAAGC CAATATGCAT TGCGGCCACA AGGTGGCGCG TCTGGGCCTG GCAAACCCCT 660 GTGCTGCCTT TTCCATGAAC ACAGGGACAA CCTCCGCTCC TGCTGTGGCT TGAGGTGCTG 720 AGTGGCGGAG ACGCCTATGT GGCTATGAGA GGGCACAAAT CATTGTCCCT ATGTTCGGAG 780 AAGGAAATCA GGTCAGGAAA GGTTAAGGGG CTTGCAGTTC CCACAATTTT TTTTTCTTTG 840 AGACGGAGTC TCGCTCTGTC TCCCAGGCTG GAGTGCAGTG GTGCGATCTC GGCTCACTGC 900 AAGCTCCGCC TCCCGGGTTC ACGCCATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGACT 960 ACAGGCACCC GCCACCTCGC CCGGCTAATT TTTTTTTTTT TTTTTTTTTG TATTTTTAGT 1020 AGAGACGGGG TTTCACCGTG GTCTGGATTT CCTGACCTCG TGATCCGCCT GCCTCGGCCT 1080 CCCAAAGTGC TGGGATTACA GGTGTAAGCC ACCACGCCCG GCCCCACAAT TCTTTTCTTG 1140 CAGCCTGAAA TTAACCCTTA GACCTTAGGC 1170
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