Tag | Content |
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EnhancerAtlas ID | HS108-38734 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:10671220-10673050 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr8:10671876-10671887 | GACAGCTGCTG | + | 6.14 | NFIC | MA0161.2 | chr8:10672925-10672936 | TACTTGGCATA | + | 6.14 | Tcf12 | MA0521.1 | chr8:10671876-10671887 | GACAGCTGCTG | + | 6.02 | Zfx | MA0146.2 | chr8:10672695-10672709 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38310 | chr8:10670179-10672864 | HUVEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I010812 | chr8 | 10670372 | 10672454 |
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Enhancer Sequence | GTGAAGAAAA GGAGAATTAT TTTGCCAGGA GCCCATGCCA GAAGCATGCT AGACAGAGAA 60 ACGAAGTGAG AATGCTGGTA ACACATTCTC CATCCTCACT CTGGTTTCGG AGTATTTTCT 120 CTAGTGATAA GGCTCAATCC GGAAACAAGC TGGAGAGAGG AAGGAAACTG GGAAGGTGGG 180 GGAGGGAAAA AAATGAGAGA GGAAAAAAAA AAAGAGTAGC AGGAAGTTCA ACCAGATAGG 240 AACTGATGGA ATTTGTTTTT CAGTGTCTCC AACTTCAAAT TGCAAACCAA GTGAGAGAAG 300 ACACACGCTT ATGTACACAG GCCCCGGCAG GCACCGGTCA GCACAAGTAC CTGCTGCAGG 360 TCTCAAGGGG CCCTGGGAAT CTCAATTCAT TATCTTCGAT CATTTCTTTG TCTCCACAGA 420 AAGTGCATAC ATCTCCAATT TAGGTGCACT CCAAACCAGT TATTATCTTC CAAATCAATA 480 TACAACAAAG ATGGTGGGAA AAGGAAGAAC TTGGAAATTA GAAATGTGCA ACCAGCCGTC 540 CCCACACAGA ACAGTTTATG AGAAGTTTTC TGAGCAACTG GCAGTTCGTG ATGATCTTTC 600 ACCATTGAAG CAAGTACTTC TGAATAGCCG GATTCAGCAG GGAAACAGCG CCTCCTGACA 660 GCTGCTGTGT CTGGAGGAAA TACGAAGCAC CAATGAAGTC AGAGGAGAGT CCTTCAAGCA 720 GTAGGAATGC TTTATCTTCT GAGCAATGAA AAACAGCCAC AGCTGTGAAA AACTATTCTA 780 GAGTGAAATG CAAGGTCTGA AAGCCAGTTT CTGGCAAATT GGATTGATTT TTAAAAACAT 840 AAAATGGTGT GAGCAAACAT TTATTCAATA ATCCTTTCTC AAGAATCCAC AAGTAGATTG 900 TGCATGGCGT AGAATGTAGA TTATGAGTAC TTCCTACTCT CAGAGAAGAA ATACTTATTT 960 ATTAGAACGT TTCAAAAGGA AAAGACATTT CAAATATCAA CCATGATGCT ATACAAACCA 1020 TGATTTTTAT GGCAACAAAG TCCATTTTTT AAAAAGAGAA GAATGATGAG GCTTCAACTG 1080 ACTGAATCCC TACCACGTGC CAAGCACTGG AGCCAGTCAC ATGCTGGGGA CCCAGGAATG 1140 AGAACAAAAA TCCTCTCTAA GGTGTTCGCT AGCCAGTGTA TGCCACAAAT GAAAAAGTCC 1200 ACATGTAAAA CACAGTGAAG CAATTTCTTC TTTTTCTTCG TTTTTTTGAG ACAGGGTCTC 1260 ACTCTGTGAC CCAGGCTGGA GTGCGATGGC GTGATGATAG CTCACTGCAG CCTCAATCCC 1320 CTAGACTCAA GCAATCCTCC CATCTCCAGC CTCCTGAGTA GCTGAGACTA CAGGTGGATG 1380 CCACTGAGCC TGGCTAATTT TTTAAATTTT TGGTAGAGAC GATGTCTCAC TATGTTGCCC 1440 AGGCTGGTTT CAAACTCCTG AGCTCAGGCA ATCCTCCCGC CTCGGCCTCC CAAAATGTTG 1500 GGATTATAGG CACGAGCCAC TGTGCCCAGC TAGCAATTTC TTTATTAGAC GCAAAAAGGT 1560 CAGAGAGAGG ACAGAAAGCA TGATTTAAGT TTCATAAACA TGTCCTAGAA ATCTTGCATT 1620 TAGCTTGGAT TGTTGTTTCG CTTTGATATA ATTTTCTTTT AATTTCTATA CATTATATTC 1680 AAAATAATTA AGAGAGCACA TTCTTTACTT GGCATAGTTT GTTCCACTAC ACAACACAAA 1740 GTTCATTCCT ACTATGCGCA CAAAGAAAAT TTACATTTTA AGTAATTTTT TTTTGAATGA 1800 AGACTTTTAA ATGCATAGTC TTAGATTTTA 1830
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