Tag | Content |
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EnhancerAtlas ID | HS091-00165 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:3727350-3728640 |
Target genes | Number: 12 | Name | Ensembl ID |
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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 | chr1:3727626-3727645 | CACTGCCCTCTGCTGGCTG | - | 7.37 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I003811 | chr1 | 3727925 | 3728364 |
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Enhancer Sequence | GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GAATCCCTTG AACCCGGGAG GCGGAGGTTG 60 CAGTGAGCCG AGATTGCACC ACTGCACTCC AGCCTGGGTG ACAGAGTGAG ACTCCGTCTC 120 AAAAAAAAAA AAAAAGTTCC CCTGCCTGGC CCTGCTCCAG GGCTTCATTC TCAGGAAGCA 180 CGGATGCCCT GGGAACAGCA GAGTTTGGAA GATGCTCTGG TGGGAGTTTG CAGCTGGGTG 240 GGTGGGCAGT GGGGGCTCCC CTGCCTTCGG GCTGCCCACT GCCCTCTGCT GGCTGGGCCC 300 CACCTCAGCT GACCCTCAGA AGTGCTCCCC ATTTAGGGGC AGGTGCCTGA CACCCTGAGG 360 CCAGCTGTGC AGAGGGCTGG AAAGTGCCTA GAGTGTGTGT CCTCTTCAGT GCACAGCAAA 420 GGGACCCTCA GTTCCATTTT ACAGGTGAGG AAACTGAGGC AGCGGCAAGC TGTGGTCAAA 480 CACTCCCTGG TAACTGATCC ATCAGTGGAG TCAGGATCCC CCATACTATT TTCAAGATCC 540 AGAGAGTGCC AAGGTTCCTC TGGACCAGCA CCTTCCTCCC TGCAGTCAGA GGGCAGCGGG 600 GGCAGCTTTG TCCTGCAGCT GTGGCTGTGT GTGCCTGACC GCTAACTCTC TACTCTGTTG 660 TTGAGGATGA CAACACCGGC CTTGCATGGT TGTGGTGAGG ATTCCGCGGA CCCGCCTCCG 720 TCCCGCTGGG TAGTCTAAGG CCACACCTCC CCGCAGGGTA GGCTCACAGG CTCACTGCCC 780 GAGCCCTGGC CATTACCCTC CTCCCACGGC TCAGCCCACC CAGCTTTCCA ATCAAGGGTG 840 CCACAGCCAC TGCCCCCGGC TTTCCTGGGC AGTAGGCAGG TGACCACCGT ACAGTGCTTA 900 GTTGAAAAGC AAAACAGCCT TGAGGGCTGG TAAAATCCCT CTTTCAAAGG GGGGAAAACC 960 CATGAAGAGA CTAGAAAGTA TAATCCTCTA CTGGGCACAA TTAGAGAACT TAGAGAACAT 1020 TCTGAATTTA TTCCACAGGA TGAAACTGGT CAATCATTTT CTCTAATCTC CATGTGGCTT 1080 CAAATTGTCC AGTTTCTTCA GCAGTGAACT TGTTTTGACA AATTACTTAT TCTAGGGACC 1140 AAACCCTCAG GGCAACTTCA TATTTGCCGT GTCTTTTTTC AGCAATTTTC AATCTACTTT 1200 CTAAGGTTTC AGGGCTGGGC TACACTTCCA TGTTTATTAA AGTAAATGTA ATTGACAAAT 1260 TACTTTTTAA TTGTAATGTT GAAATAAAGT 1290
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