Tag | Content |
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EnhancerAtlas ID | HS091-08903 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:120100650-120102340 |
Target genes | |
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) |
ZNF263 | MA0528.1 | chr11:120100784-120100805 | GAGGAAGGAAGGAGGAGAAGG | + | 6.03 | ZNF263 | MA0528.1 | chr11:120100788-120100809 | AAGGAAGGAGGAGAAGGAAGA | + | 6.19 | ZNF263 | MA0528.1 | chr11:120100791-120100812 | GAAGGAGGAGAAGGAAGATGT | + | 6.36 | ZNF263 | MA0528.1 | chr11:120100787-120100808 | GAAGGAAGGAGGAGAAGGAAG | + | 6.42 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59639 | chr11:120094297-120131709 | Ly4 |
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Enhancer Sequence | CTAATGAGAC CCAGAGTTTG GAGAAAACTT TTGGCCAATG CTGCCACCTG ATGTCAGAAA 60 GTGTCCCCAC ACCCTAGCAG TGGCCTATCT TGGAACAAGA ACTTCGAAAG CACCTACTGT 120 GTGCTCAGCC ATTTGAGGAA GGAAGGAGGA GAAGGAAGAT GTTACTAGGG AAGGATGAGA 180 TAAAACTTCT GCACCCAAGA CAATGAGACA GACATAGCTG CAACCGTAGT AAGCCAGTCA 240 GAAATAGCCA GCGCGAAGGC AAGAGATGGG GTGGAGATTG GAACCCCGCT TCAGATCTGG 300 GCTCGGCTAC TTACCTGCTG TGCAGCCATG GGTCAAGTTG CTTGACCTCT CTGTGCCTCC 360 ACTCCCTTAG CTATAAAATG AGCTTACTTA AGAGACCGAA GTGAATTCTT GCATGTCAAG 420 CATCTAGCAC ATAGTGCTGT TAGCCATTCT TAGTATCATT ACTATTAGTG AAAAAAGCAG 480 ACATTCCTGC AGCTATAAGC CTGACTCAAT GAAATCAGAC ATCTGGAAGG CTCTTCACTT 540 CCAAAGTATC TTTCAACATG AAGAGGCTGT AATAGGAAGT GCCGGGCAGG GTTCTGGATG 600 GTTCCAGAGC GAGGGATGTG CAGGCTGCAT GTATTGGGAA AGGCTTTCTG GAAGAGTTGG 660 GGTGTGGGTT GAGGCTGGAA GATGGTAACG ATTTGGCAAG GTGGAGGCAG GAGTGTTTTA 720 GGGGTTGGAA GAGTCTCATG GGTTCCCCAG GTGACCCAAC TTTCTCAAGG AAGAGATGGG 780 GACAGTCAGA TCCTTCCTTG AAGGCCTTGG CGAGGGAAGG GGTTTGCAGG GTGGTCCCCT 840 TTACTCTGCT CCCAGAACTC CCAGAACAGG CTGCAACTGC CCCTTGAACT CATGCAGGCC 900 AGAGGGTTGA GGGAGCTGGG CTTGCTTGGC CTTGGTTGAG CTGAGGGTCA GCGGGGAGAT 960 AACCTTTTCA GGTGGGCACA CCTCCCTTCT GAACCTGTTT TCAAGGACCA GCTCAGCCTT 1020 GCTGGGGGAT GGGGAGGGAG CTGTCCCATC AGTCACCCCC CAGTCCTTTT TCTCCTTCCC 1080 TTTCTGCCAG GGCCTCCATC CCAAGCCCCA GCCATTGCTC CAGGTGGGCA AGGGATACTT 1140 GGAGAAGGCA CCTGCTACCT CCTGTGTGCC TTTTTTGATG GAAGGGGAGT CCCCAAATCA 1200 GTATGTTTTC CCTTCTGATT TCCAAGTCAC CAAAAATAAT GCTTTTTTAA AAAGCAATGT 1260 TTTCAAGACT TGGAGTGTTT TTCTGACCTT CCTTGACTAG CACCTCCTAG CTTGTCTGGC 1320 CCCTGCAGTG AGGGGGCTCT GGACACCATC ACTACAGACA CCAGCTGCCT TGGGCTCCTT 1380 AGTCTCAGGG GATGGTGATG AGAAGAATCC CTGAGACTTT GGGCTGACCT TAACACTCTG 1440 CAAAGTAGGC ACCTCCCACA GGGCCACATC CAAGGGCTCG AGTCCACCAT TCCAAAGCAC 1500 TCGCCCAACC GCCTTAGCCC CACTGTCACA GCACCTGAAA TCCTGCCGTG ACAGTCACTT 1560 CTTTGCTGAA AAGCAAATTT TAGTGTGCAT CAGAATCACT TAGGAGCTTG TTGAAATAGA 1620 TGTAGGTGGT CAGCTGTTTG GCAAACACTG AGATAAGACT TCCCTATCGC AGGAGGCTTT 1680 TGTGGCCGTG 1690
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