Tag | Content |
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EnhancerAtlas ID | HS034-04699 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:2751770-2752860 |
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) |
HNF4G | MA0484.1 | chr11:2751852-2751867 | TGGACTTTGTCCCTA | - | 6.23 | Hnf4a | MA0114.3 | chr11:2751850-2751866 | GGTGGACTTTGTCCCT | - | 6.62 | ZNF263 | MA0528.1 | chr11:2752029-2752050 | AGAGGAGGGAAGAATGGAGGG | + | 6.64 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35355 | chr11:2747987-2755117 | HepG2 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I002724 | chr11 | 2745822 | 2753258 |
|
Enhancer Sequence | TCTGGAGGAG CCGGTCAATA GCAGCGTGGT GGGGTCTGGC AGAGACAGAC TGCAGGGGGC 60 CTGGGAGGCC CCAGGAGGCA GGTGGACTTT GTCCCTAGGC ATCCAGTGCA GAGGTGAGAC 120 CTGTATGGCC ACAGAGTCTC CCTATCCAGG CCCCATTACC CTGGGGGAGG CGGATTATGG 180 TATGAACTGC TGCAGGTGGT CCAAGAGGGG CTGCCCCTGG GAGACGCAGG GTTCTTCAGT 240 AATGGTGGTT TCGAAGGGCA GAGGAGGGAA GAATGGAGGG ATGGGGGACA GACGCTGGAG 300 CCGTTTTGGT GGCAGGCCTC TGTGGCTGTG GCCAGAAGCA GGGCTGGGCA CCAGGCCAGA 360 TGGACCAGAG GCTGCCCCCA GCTGAACCAA CTACAGAAAT GAGAGCCCCG GCCCAGCCTC 420 CTCCCAGCCG CCGCTCTCTG GGAGCCCAGC TTTGCTCATA GAAAAGGAAG GCCCTTGTTG 480 CCCTGCATTG GGAGCAAACA CTTCCTTTGG CCTCACAGCT CAACCTTGGA CCCAAAGGTC 540 CTCAGGGACC TGGGGGAAAG AGAGGGCAGC CAGGCACCTC TGTTCACGGC AGGGGCTGCG 600 TTGCCCAGCC TGGCAGAGGG AGGCAGCCCC TAGGTACAGT CCCCTGTGCC CACTCGAGGG 660 GGTGCTGAAT TCCTCAAGGC CTGAGTCAGA CCTGGTGCAG CTTCATAAAG CCAAGGGTGG 720 CAGGCGGAAT CCAAGGGGCC TCACCGCCCA TGCACCCCAC TGTTGCATGG AGAGAACAAT 780 GCCCAAATGC CCTCGTCCCA CAGTCGGCAT GCCAGACCCC TCGGGAATTC AGGCCTTGGT 840 GAGTCTGGCA CATTCCGGCT GTGTGTCAGC GGGAGAGGCC TGGGAAAGGG AGCCAGCACT 900 GCAGGCCGCC CACCACACGC CCACTCGGGC ACCGGACACA GGGAAGGCGG ACACCCAGGG 960 CGGCCATCTC TCGGGACAGG AGGTGCGGCT CCAGGTTCTC ACCCAGGAGA GGGCTTTCCT 1020 CCCATGTCAG AGTCCCCTTC GCTGCTTGAG GCAAGCCCTC CGGAACAGAC CCATCTTTTG 1080 GGGGACCCTG 1090
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