Tag | Content |
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EnhancerAtlas ID | HS091-03350 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:170658280-170659680 |
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 | chr1:170658843-170658862 | TGGGCACCAGGTGGCGATA | + | 6.29 | ZNF263 | MA0528.1 | chr1:170659248-170659269 | TCCTTACTCCTCCCCTCCCCC | - | 6.41 | ZNF740 | MA0753.2 | chr1:170659261-170659274 | CCTCCCCCCCCAT | + | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_45625 | chr1:170630571-170666837 | Osteoblasts | SE_56260 | chr1:170657928-170658730 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I170688 | chr1 | 170657929 | 170658730 |
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Enhancer Sequence | CAGTAATAGA GGACCTTTAT TTTTTTTTCT GTTATTTCAA AAAGATTAAT AAAAATGTAT 60 GTTTACTCTC TATAAGCAAA AGAAGAACTT AAGATTTTTG ACAGGATTGA TAATAATTTA 120 GTGAGACTCT TTCTGTGGAG CTGTGTACTG TTCTTAGAAC AAAGTAGGGA CTCATTAAAG 180 AGCTGAATAA GTCAATGAAT GAACAATATT CCTGGCTATC TCAGGCTAAA TGATATCATA 240 GTCTGACAAT TTTGAATTTA CTTAATGCAA ATGACAAAAT ATAGTTGATT TAGTAGAAAA 300 GGTTTTAAAT CATGGAATCT ATGTGGGAAG GTAGTCCATG GGGCTGCAAC AATTGAGAAC 360 ATTCATAAAG ATGTGAGTGG AAACAAGGGT GAGTTTTGAG GAAGATTTGT GTGTTTAATC 420 TTTATATGCC TGTGACCAGA TGTCTATGCC AAGAAGCACA TGTTTTTGTT TTTGTTTTAA 480 ACTTTCAGTT TATGGTTCCA AGGTCCTGAT ACTTATCAGC TTTAAAAAAA TCGTTTTCAT 540 TTTTTAGGTA GTTTTCTTGC TTTTGGGCAC CAGGTGGCGA TATGGAGTGA GGTGGGGAGT 600 GCATGGGATA CACAGGTTGG GTTGTCATAA AGACCAAGCA TCTGTAGAGC CGAACTGATG 660 AGATTTAATA TTCCGTCTCT CTCTCTCTCT CTCTCTCTCC CTCTCTCTCT CTCTCTCTCT 720 CTCTCTCTCT CTCTCTGTGG GTGTGTGTGT GTGCGTGTGT GTGTGTGTGT GAGAGGGAGA 780 GAGATCCAAA AAGAGAAAAC TTTGTAAAGA TTTGGTTCCA TTTTGTCTGA GAAAGACTGG 840 ATTGGCATTC CTCATCTGTA TGAAACACTT CTCAACAGAT TCCATACAAT ATATCGCTTG 900 GAAAATTCAA GAGCTGCCAG GTCTCTAGCT CTTGCTAGCA TTTGGTTAGC ATTTCACTGT 960 ATATAAGATC CTTACTCCTC CCCTCCCCCC CCATTTTTTC AACATTTACT GAGCACCTAT 1020 AATGTCCCAC GCACTGTAAT AAGTATTAGA AATATTGCAT CAGATAAGGT CTGGTCCGTG 1080 CCCCCTATGA GCTTATAGTT TAGCAGAGAT AGACATATGA ACCCTAAATC AGCTGCATGT 1140 TATGGCTTCT GCGATGGAGT CAGGATCAAG GCAGGATATA GAAGGGTCAC AAGGATGAAC 1200 TTGTCAGCTC AGTGGGTAAA GAAAAACATC ATGGGAGATA TGAACTATAA GCTGAATAGT 1260 GGCAGATGAG TAGATATTCA TCACTTAGAA TAGACTTGGA GAGAGAAGTT ATAATAATCA 1320 ATTTTGCTCC TTTGAACCCT TCAGGTGTGT GTGGTGCGTA TGAGAAAGTC AGTTGGATCT 1380 TAGCATTTAT TTATAATAAT 1400
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