Tag | Content |
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EnhancerAtlas ID | HS091-05571 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr10:73143100-73144750 |
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 | chr10:73144143-73144162 | CGGCCTGCAGGTGGCGCCC | + | 6.88 | Nr2f6(var.2) | MA0728.1 | chr10:73143173-73143188 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09827 | chr10:73141153-73143535 | CD14 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I071384 | chr10 | 73144061 | 73144250 |
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Enhancer Sequence | TCTTTGGGGC CGGGTGCAGT GGCTCACACC TGTAATCCCA ACATTTTGGG AGGCTGAGGT 60 GAGTGAATCA TTTGAGGTCA GGAGTTCAAG AGCAGCCTGG CCAAAGTGGT GAAACCCTGT 120 CTCTACTAAA AATACAAAAA TTAGCCAGGC AGTAGTGGCG CACGCCTGTA ATCCCAGGTA 180 CTGGGGAGGC TGAGGCAAGA GAATCATTTG AGCCTGTGAG GCAGAGGTTG CAGTGAGCTG 240 AGATCATGCC ACTGGACTCC AGTCTAGGCG ACAGAGTGAG ATGCTGTCTC AAAAAAAAAA 300 AAAAAAAAAA GACTCTTTGG ATAGGCACCA TCAACCCATT TTACAGATGA ATTAAATGGG 360 GCACACAAAA GTTAATTAAG TTGCCCAAAG GGTGACACAG CAAGGAAGTG GCACAGGTGG 420 GATTCAAATT CAAGCCTACC TGACTCCAGG CCCCACAATG TTGCCTCTAG TTGTTACCTG 480 CATTTTATAA TAAGGAAGGC AGCCAAGGCC CAGAAATGGG CAGTGATTTT CCCAGAGTCA 540 CACAGCCAGC TAGTGGCTGG GCAGAGACTG AAACCAACAG TCCAGACTTC CAGTTCCAAA 600 ATGAGCCCAT AAAAGTACCT GGCCCGTAGG AAATCTTCAA GTCGTATTTG TTTTTTCATT 660 TGTTTTTCAT TTTTGTTTTA GAGACAGGAT CTCACTCTGT TGCCCAGACT GAAGTGCAGC 720 GACACAAACA TGGCTTACTA CAGCCTTGAC CTCCTGGGTC AGGTGATCCT CCTGCCTCGG 780 CCTCCCAAAG TGCTGGAACT ACAGGCATGA GCCACTGCAC CCAGCCATCC ATTAATATTT 840 GTGATAGAAA CAAGGCTAGG GAGAATCCCT GGATGGCTGA GGATAGGGGA GCAGCGGGGA 900 GGAGCAGATG GTAAAGAACA GGCCTTGCTG GAGACCACCA ACCTGCTGCT TTTTTCTAGG 960 AGTTGCCCTT TAGCCTTCCC TTCAAAGTAG GGCTTGGGGA GGTGACCCAG AGCTGGGAGG 1020 GGTGAGAGGT GTCGTGCAGC ACTCGGCCTG CAGGTGGCGC CCCACACTGC AGTTCTGTAC 1080 TCCCCCAGGG AATGGGAGCC TGCAGGGGAT TTTCCTGTGG CTGGGCGGGG TGGGACCAGG 1140 GCAGTGGGTC TCTCACCAGC GTTTTCAGGA TGCCCCTAGA CAACAGCTCC CCTCTCACCC 1200 TGGCCGCCTA TGCCTGGCTG TGGCTGTGGC AGCAGATGGC TGACAGGGCC CAGATGGGAA 1260 CTCACACCTC AACTCCTTCC TCCCTGGTCA TGCCCTCTGC AGGGCCCTGG GTGAGAAACC 1320 TCAGAAGGAC TTGAGGTCAT CCAGCTGCTT GACCTTGGCC AGTTTACTGA GCCTCTTGGA 1380 TGCCTACTTT CTTCATCTGT AGAGCAGAAG TGGGTTTTAT TTCCAGGGTA CTGGGAGGAT 1440 CAGATGGAAC ATTTATAAAA TGCCTGGCCC AGGCTGGGCA TGGTGGCTCA CACCTGTAAT 1500 CCCAGCACTT TGGGAGGCTG AGGTGGGCGG ATCACGAGGT CAGGAGTTCG AGACCAGCCT 1560 GGCCAACACG GTGAAACTCT GTCTCTACTA AAAATACAAA AATTAGGGCC GGGTGCGGTG 1620 GCTTACGCCT GTAATCCCAG CACTTTGGGA 1650
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