Tag | Content |
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EnhancerAtlas ID | HS091-45218 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:150869640-150871050 |
Target genes | Number: 13 | 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 | chr7:150869781-150869800 | GGGTGCCCTCTGGTGGCAG | - | 7.64 | ZNF263 | MA0528.1 | chr7:150870512-150870533 | CCCCATTCCTCACCCTCCTCT | - | 6.13 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I151172 | chr7 | 150869741 | 150869890 |
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Enhancer Sequence | CCTGACCTGT GTTGCCAACC AGCACCAAGG ATGCTAAGAA AAAAACAAAG TATTCAAGTC 60 AAAGACCACA AATCTATACC TCCAATCCAC TCATTGGCCA GAGAAAGTCC TCTCATGGTG 120 GGCAGCGTCG GGCCTGGCCG CGGGTGCCCT CTGGTGGCAG CAGCGCACAA CTGCGGGCAC 180 GGCGAAGGAG GTGCGGGGTG CTGCAGCGCC CCCTGGCGAC AGTCCAGGAG ACGCGCCGAG 240 GGCAAAGAAA CCACTAACGG AGCATCCAAG GGCGAGCGCG CGGGACGCCT CTAGATGCTT 300 AACTGTGAAT GCACTGTTTG GGGACGGGGG GTTGTACGTG AGTGTCTTAA CGTCTAGTGT 360 GCGTGAGTGT AGGGTTAAGT ATGTTTAGTG TGCCCCGGTA CCCGAACCCT GTATTTCTGT 420 TGTGTTAAAT GTGTACAGTA TGTATGAGCC CGCGCGTTCA CACGCGGGTA GGTTGGTGGT 480 GGGGAGGTCC GCGCCTCAGT GCAGGGCGGA GTCCTCACGG AGGCGTGAAA TTGGTTTGGA 540 GCAAACACAT TACGAAAAGC AATTACCAGG GAGAGGTTCT GGGCCCGCGG GACCAACAGC 600 CAGGAGGCTG GGGAGGGAGC GCCCTGGCTC GCAAGAGTCT GAATGTCTAA CCCCAGTGAG 660 GACCCTCCTG ACATTGCCCG CTAAGGGGAC AATATGTGAA GTTGTGCACA GCCCCTTCAC 720 AGCCACCACT CCACATCGCC TTTCTTCCCT TCCCCGTCCT TAAAAAGGCA TCCCATGATC 780 GCAGGCTCTC CAGATGTGGC CAGAAATCCT CCCCCATCTT CCTATCACTT TAGAGGAGGG 840 TCCTTCTTCT GGGACGCCCT CCCAGATCTC AACCCCATTC CTCACCCTCC TCTTCATGCC 900 CCCAGCTCCT GCTCCCACGT TTATCTTGCA TTCATCCTAT TGCCCCTTGT ATTCTAACTG 960 GTTGTTCACA CCCTTGTTTC TCAGACTAGA CTGAAGATTC ACTGAGGGCA GGAGCGTGTC 1020 TCGTTCCCAG CAGGGCATGA AGCACCTAAA ACCTGGGGAC CCGGAAGCAC ACAGTGAACC 1080 AAGTGGGTGC GATCAAATAG AATTTCCATC AAAATCCACC AGCAGGACTC TCTCGGGCAA 1140 GTCATCTGCG GGAGTCGGGA TTCCCTGGGA GCAGAGCTCC AAACTCTTTC CCGCACCAGC 1200 GAGCCCGCAC TCGCATGATA CCCAGACCTG CGCTCGACCT GGCCCCAGAT CCCCGTGCCA 1260 AGGGCCACAG CCTCTGAGAT GCTTCCTAGG CGGCTCCAGT GCCATCTCCC CAGCAACGGC 1320 CTTCTGCTTC CCGTTACTTC CTCGTCTTCC CCATCTTAGC ATCTGGCACC ACCGTCCAGG 1380 GGTCCAAGCC AAAAACCTGC GAGTCGCCCT 1410
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