Tag | Content |
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EnhancerAtlas ID | HS091-30721 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:34164750-34166750 |
Target genes | Number: 35 | 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) |
CEBPA | MA0102.3 | chr20:34166576-34166587 | TGTTGTGCAAT | - | 6.14 | IRF1 | MA0050.2 | chr20:34166033-34166054 | TTTTACTTTTTTTTTTTTTTT | + | 6.16 | IRF1 | MA0050.2 | chr20:34166027-34166048 | GTTTCGTTTTACTTTTTTTTT | + | 6.18 | MEF2A | MA0052.3 | chr20:34165552-34165564 | TCTAAAAATAAA | + | 6.07 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I035575 | chr20 | 34162958 | 34165177 |
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Enhancer Sequence | CTGAAATTAA AGAGCAGATC CAGAGATTCT TCCCCATCCC CTTCAACCCC TTAGTCTACC 60 CCCTTTTCCA GGAGAGTTGG GAAACCTTCA CTCAAGTTCC CACTGTGTAT GCCACTTGCA 120 TTTTTAAAGC TCCAATTTAT CATCCAGCCT GCCCTGTCTA GGGCAGTCAC CACCAGCCAC 180 ACGTGGCTAC TGAGCAGTCA AAACGTGGCT AGTCTGAATT GCAATGTGCT GTAAGTGGCC 240 AGGCTTGGTG GCTCATGCCT GGAATCCCAA CACTTTGGGA GACTGAGGTG ACTACTTGAG 300 GCCAGGAGTT CGAGATCAGG CTGAACAACA CAGTGAGAAC CTGTCTCTAT GAAATAAATG 360 CTTTTTAATT TTTATTTATT TATTTTTGAG ACAGACTCTT GCTGTGTAGC CCAGGTTGGA 420 GTGTATTGGT GTGAACATGG CTCACTGTAG CCTCAACCTC CGAGGCTCAA GTGATCCTCC 480 CACCTCAACC TCTTGAGTCG CTGGGGCCAC CGGCGTGTAC CACCATGCAC AGCTACTTGT 540 TTTCATTTTT AGTAGAGATG GTGTCTCACC ATGTTCCCCA GACTGTTCTC AAACTCCTGG 600 CTTCGAGTGA TCCTCCCACC TCAGACTCCC AAAGTGCTGG GATTACCGGC ATGAAACACC 660 ACACCCAGGA AAAAAAAAGT TTGTAATTAG CTGAGTGTAG TGGTATGTAC TTATGGTCCT 720 AGCTACTGGG GAGGCTGAGG TGGGAAGATC ACTTGAACCC AGGAGTTTGA GACCAGTCTG 780 GATAACAGAT AAAGACCCCA TCTCTAAAAA TAAAAAGAAA AGAAAGAAAA AGATGTGCGA 840 TAAGTATAAA ATAAAAACCG GATTTTTAAA TACTTAGTAC AAAAAACAAG AATGTAAAAT 900 ATCTCAGAAA TTTTATGATT ACTTGTTGAA GTTTTTTTTT TTTTTTTTTT TTTTTTTGAG 960 AGACAGAGTT TCACTCTGTC ACCCAGGCTG GAGCACAGTC TCGGCTCACT GTAACCTCCA 1020 CCTCCCAGGT TCAAGCGATT CTCCTGCCTC AGCCTCCAGA ATAGCTGGGA TTAACAGGTG 1080 CCCAGCACCA CGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CGCCATGTTG 1140 GCCAGGCTGG TCTCGAACTC CTGACCTCAA GTGATCTGCC TGCCTCAGCC TCCCAAAGTG 1200 CTGGGATTAC AGGCATGAGC CACTGTGCCC AGCCTTGAAA TGGTATTTTG AATATATTAC 1260 TAAAATTAAT TTCACCTGTT TCGTTTTACT TTTTTTTTTT TTTTTTTTTT TGAGAGGGAG 1320 TCTCGTTCTG TCGCCCAGGC TGGAGTGCAG TGGCGCAATC TCGGCTCACT GCAAGGTCCG 1380 CCTCCCAGGT TCACACCATT CTCCTGCCTC AGCCTCCTGA GTAGGTGGGA CTACAGGCAC 1440 CCGCCACCAT GCCCCGCTAA TATTTTTTGT ATTTTTAGTA GAGACGGGGT TTCACCATGT 1500 TAGCCAGGAT GGTCTCAATC TCCTGACCTC GTGATCCACC CGCCTTGGCC TCCCAAAGCG 1560 CTGGGATTAC AGGCGTGAGC CACCGCGCCT GGCCCCTTCT ACTTTAATGT GGCTACTACA 1620 AAAGTTAAAA TTACGTATGT GGCTCGTGTT ATGTCTTTTG GACAACACAG CTCTAGATAA 1680 TGGAGTTAAT AATCCCCAGC TTCTAGAATT GTGAAGAAAA GAGGACTATA ATGAAGAGCT 1740 CTGAAAAACT GTAGAGCTCC ACCTTCAATG AGATCATTCT TGTTTTTTGT TTGTTTTTTG 1800 AGACGGAGTC TCACTGTCAC CCAGGCTGTT GTGCAATGGC ATGATCTCAG CTCACAGGAG 1860 CCTCTGCCTC TGGGTTCAAG TGATTCTCCT GCGTCAGCCT CCTGAGTAGC TGGGACTACA 1920 GGTGCGCGCC GCCATGCCTA GCTAAGATAT CATTCTTTTT ACCATTTACA CCCCAGCCCC 1980 CTCCCTGGGA CCCTTCTCTG 2000
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