Tag | Content |
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EnhancerAtlas ID | HS113-18513 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr2:2848740-2851150 |
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) |
DUX4 | MA0468.1 | chr2:2848916-2848927 | TGATTGAATTA | - | 6.14 | EBF1 | MA0154.3 | chr2:2849620-2849634 | AATCCCCAGGGAAA | + | 6.05 | POU2F2 | MA0507.1 | chr2:2851060-2851073 | TACATTTGCATAT | + | 7.12 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33649 | chr2:2847186-2856385 | H2171 | SE_66981 | chr2:2847186-2856385 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I002846 | chr2 | 2849874 | 2851350 |
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Enhancer Sequence | TTCCACATGG CTGGGAGACC TCAGGAAACT TATAATCATG GAGGAAGGCA CCTCTTCACA 60 GGACAGCAGG AGAGAGGATA AGAGCCAGCA GGGAAAATGC CAGACGCTTA TAAAACCATC 120 AGATCTCGTG AGAACTCACT CACTATCACG AAAACAGCAT GGGGGAACCA TCACCATGAT 180 TGAATTACCT CCACCTGGTC CCACTCTGAC ACGAGGGGAT TATTACAATC CAAGGTGAGA 240 TTTGTGTGGG GACACAGAGC CAAACCATAT CAACCTCAGA CCACCGCAGT CAACAGTGCA 300 GCCAATGTTT CCTGGAATCG TTGAGCAGAC ATCAAATGGA GTAGCTGCCT TTTGTGTAGA 360 GGCTGTGGTA TGGATGTCTC TACGTTGGAC CCACACTTGG CATCATGCAA GTCACACCTA 420 TCAGACGCAT GACAGAGATG AAGCCAGCTG GTCCCGAGCG TGCCTATGCC TGTCCATGTC 480 TGTGCTGCCT CGCTGCAGGC ATGCACTCTC CTGCCGTGCG CTGAGGTGGA CGCTGCATGG 540 CTGGGACATT CTCTCTACCT GTCTCTGCCT CTGTGTCTGT CTGTCCCCCA CACACACATG 600 TGCGTACACA CACAATGTTG CTGGTCCCTG TCCACTAGAA TGCACTCCAT GTGATGACTG 660 TGGATCCTAC CACGACCAGC ACCAGAAATA AGGCACCAGC ACAGCTCAGG AGAGGAACTC 720 GCCCAGGTTT TGAAAGATTT GATCCATCAT CCTCACTTTG AGTACAAGTC AAAAATAAAA 780 ACCTCCAGAG GCCAACCCTT TTTAAAATTC ATTTCTTATT GCCTTTCTTT TTTCTCTCCT 840 TTTCCTCTCT AGATGGTGGC AGCAAAATTC AAAGCAAGAG AATCCCCAGG GAAAGGACAA 900 GATGGCAAGA CCCAGCCTGG GGTGGCCACG GCCCTCCTCT CTGACAGGAT CCTTCCCTGG 960 GAGGTTTTCT CTCAACTTCT ACACCCAGAA CTGTCTCCAA AACGGGAAGC GTGTTAGCTG 1020 GAAACGACTC GTTCCTAGCA AGGCTGCTCC ATCTGCATGG GCTCGGCGCT GCTGGGATCT 1080 GGGATCCGTC CTGACTTGTG ATTCTGGTGC TGTTGCCTTG GGATCCTCGC TGAAATGCCA 1140 GCCACTACGT TGGCTCCCTT ATAATCACCT CTTGCCCACT AGGGAAGGTA AAATAGCATC 1200 GAATCAGGAG GAGGAGGCAT CGGAAGCACT GTGATGGGGA CGTGGTTAGG TTTTCTTCCT 1260 CCAGCCCTGA ACAGGAGCCT CTGAATTTTT CAACAGCTGT CTTTGCCCCT CTTGGAGAAA 1320 GCCCCGTCTG TTCCCCCTTC CTCACTGCGT AATCCTTCCC ATACGCCCCT GCTCGCTGCC 1380 ATTTCTGAAG GACACAGGGG GCTTCTGTTA CCTGAGCCCT TTTTCCCTCA CAGATGCCTG 1440 CAGGCTGAGG CTTGCTGGGG AGGCCTCTTC AAGGGACGCC TAGCCCCTGG ACATCATCCA 1500 AGTTGGCAGC TTCACCACAG AGCTGCTGAG AGAAAGGCGC GGGGGGCAGC CTGGGCTGGC 1560 CTGCTGAGCC AAGATAAAGC TGCAGGAACC TGCTGCTGCC AGAAGGGATG TTTGCTGGGT 1620 TCCCACAGGT GACCAATGCA GGCAGAGACC AGCCAGGACT CCAGCTCAGG GACAGTGATG 1680 GGCACAGGGT CACGCAGGGC TCTAGGCTTG GCCCAGGTTT TGAGCCAACA ACACCAGCTG 1740 CCTGGTGGTG GGAACAGACA CAAGCACCAG GCTCAGTTTT CAAAGCTCTC CTCCTCCTTC 1800 TCCTGTTATT TAAGGTCATA CCACATTGGA AGTGAGTCAG GCAGGTGGAG CCCTTTATGT 1860 CCATGAGGCA GGTGCAGCAG CCCAGGGAGG CAGGGTGGCC TTTCCCAGGA ATAGCCAGCG 1920 TCACCTGGAG GCAGAGCCAG GCGAGGGCTG TGTGGGTGGC TCCCAGCCAT GTGGACAGCA 1980 GGCCTGACTG TCCCTGTCCC CATGAGCCTC ATGAAGGTGC CGCGGATCCG TCCAGGCGTG 2040 GGTGTTGTTC TCTTCCGGCC CAGCCTTCTC CCTCTTTCCA CACACACGAT TGGGCCAGCA 2100 TCTCCCGTCT GCTGCCATCT CCTCTGCTGG TGGGGGTGCG TCAGCTGACC CTGTGCCCTC 2160 TGGCCTCATT TTTCATGGGT GTTGCCACTG TCTGGCTGTC TGCCCCTTCC CACATTAACT 2220 CTCACCCTCT GGCGGCAGAG ACCTTGTCTT GCCCATCTCT GTATCTCCAG CCCCCAGTGG 2280 CCCTCAGTGC GCATTTGCCA AGGGAAATAT ATGCAAAAAG TACATTTGCA TATCACAGCC 2340 CTGTGAGGCA GACACACCCA GAATCATTGC TCCTGCTTTG CAGAGAGGGT CTGTCCCTGG 2400 ACCCCGTCTT 2410
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