Tag | Content |
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EnhancerAtlas ID | HS053-03361 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:200874150-200875380 |
SNPs | Number: 4 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr1:200874195-200874209 | AAAGATCAAAGGCA | + | 7.73 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23181 | chr1:200874081-200874690 | Colon_Crypt_1 | SE_23181 | chr1:200874811-200875442 | Colon_Crypt_1 | SE_27435 | chr1:200873387-200874956 | Esophagus | SE_27435 | chr1:200875065-200878791 | Esophagus | SE_33981 | chr1:200873398-200878744 | HCC1954 | SE_50836 | chr1:200873411-200875646 | Sigmoid_Colon | SE_52641 | chr1:200873442-200875476 | Small_Intestine |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I200905 | chr1 | 200874082 | 200874690 | GH01I200906 | chr1 | 200874781 | 200875150 |
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Enhancer Sequence | GGTGTGCCTG GCCCAATGAA AATCTTTATT CCTAAGGTTT TTATAAAAGA TCAAAGGCAG 60 GAGACCAGAA TTCAGTAAGA GGGGGTCTCT TTAATTGAAC CCTAAAGCAA AGGCTACTTG 120 TGAGCCAAGC AAAGCATGGG CTGGCTGGCT ACTCAGGAGT CAAGCCCAGC TCCTGGTACC 180 GTATGTCCTA GAAATCTACT GCCTGCTCTG GGTAAAGATT TTTTCATTAA ATTGCGGAGC 240 AGGCTGAGCA TGTTGGCTCA AGCTTGTAAT CCCAGCACTT TGGGAGGCCA AGGCAGGAGG 300 ATCTCTTGGG CCCAGGAGTA TGAGACCTGC CTGGACCACA CAGGGAGACC CTGTCTCTAC 360 AAATAACTAA AATAAAAAAA TTGGATAGGC ATGGTTGTGG ACACCTATAG TCCCAGCTAC 420 TCAGGAGTCT GAGGTGGGAG ATTGATTGAG CTCAGGAGGT CAAGGCTGCA GTGAGCTGTG 480 ATCGGGCCAC TGCACTCCAG CCTAGGCAAC ATTGTAACAA CCCATCTTTA AAAAGATGGG 540 TTAAACCTTT GTGGAGCAAA GGTTAACAAA CTTTTCCATA AAGAGCCAGA CAGTACATAT 600 TTTAGTCTTT GTAGGCTCTT TGGTCTTTAT CACAACTGTT CAACTCTGCT ACTTCAGTGC 660 TAAAACAGCC AGACATTACA TAAACAAATT CATAGCCGTG TTCCAATAAA CATTTATTTA 720 CAAAAGCAGC TATTGAACTG GATTTGACCC CTGGGCCATA GTTTGCTAAC CTCTGTTGTA 780 AGGGATTTCA AGATGGTTGG AACTTTTTAC TTTTTTTGAA ACTTCCTGGG CAATGCCCAT 840 GCATTTGAGA TGCAAGCTCA CAGGGGAGAG CCCATAAAGG GTTGTGGTTA AGAGCAGACT 900 CCAGTCAGAC TGTCTGGGTG TGAATTCTGA CTCAACCACC TTTGTTGAAT GTATAACCTA 960 AACCACGTTA CTCAACTCCT CTGAGACGTG GTTTCCTCAA CTGTCACTTG CAGGTGATAA 1020 TATCTACCTT ACGTGGTTGT TATGAGAATT ACCTGAATTA ATATATATAA AGTGCTGTAT 1080 TTAGAAATGT ATTGGCACAG TAGAAACATT AGCAATTATT ACTTTTTCCT CATCTTCATT 1140 CTCAAACACA GTTGAAAATG TTTCGTGAGT TCCATCCAGG TCACTTTAGG CTTATTCTCA 1200 AGATCTGAAG GCCTGGCCGG GTGTGGTGGC 1230
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