Tag | Content |
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EnhancerAtlas ID | HS111-03268 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr21:38090700-38092030 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr21:38091109-38091122 | TTCTAGAACATTC | + | 7.52 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26793 | chr21:38089754-38092580 | Esophagus | SE_32017 | chr21:38090453-38092619 | Gastric |
|
| Number: 1 | ID | Chromosome | Start | End |
GH21I036718 | chr21 | 38090908 | 38092610 |
|
Enhancer Sequence | TGTTGTCTCT CCTCTGATGG AGAGCCACAG GCTCCCAGCG ACACCTGCAG CAAGACACAC 60 CTAAAAATAA CAAGGGGGTG GCTCGGGACA AGACACACCA TGAGCCTCCT TTTGTTATCT 120 TGAGTTACCC TCTCTCCTTC CGGCAGGGTC AAGAAGGAAT TCTCCAGACC TACCCAAGAT 180 CCTTCGCCAC CCAAGGACGG TTTCCCACAT GCTTTGAGTT TCTTCTCAGG CTGGGCACTG 240 GGACTCCCCT TGGTGGTGGA GGAAGTCCTA CCACTGCCCC TGGGCCTCCC CTGAACAATG 300 CTGGGGTTCA CCGACTCACT GTCCTTGTCT GCCACCCTCA GCACTATTGA TTATAGCTCT 360 AAAAATAGGA TCCACCCACC ACTGCTCAGA AGGCTGCTCT GCTAGTCATT TCTAGAACAT 420 TCTGTGCCAC TGTCCATCTT AAGGTGGGTG GGGGCCCAGG TGTTGAGACT CTATCATATC 480 CTCTCCTGGT GCTTATGTTT GAGAGAACAT TCGAAAGATT CTCAAGTTCG GGAATTTGGG 540 CCTCCAGGGA CCTCTGTGTA AAAATTGTAA CTATGATGGG TATTTTCCTG GGGCCATCCA 600 TTCCTGCAAA GTGACATGGA TGTGCTGTCC TCTGTGGGCT GTGTCTGGAA ATAGGTAGCG 660 TCGGACTGTT GAGGCAGCAA CCCCAGGACA TAATCCCCAT ATAACGTGGC TCTCTGGAGC 720 AGGCCCAGAC CCTCCCGCAG GGCACGCACA GCCCCAGCCA CACCCCTGGG CGGGAGCCAC 780 AGAATTAGCA CAGTCATCTC GGACTGGGAG GGCCAGAGAC TCATTGCTGG TAATGTGAGA 840 GAGGCCTGGC AGCGCCTGAG GGGCACAGCT CAGAGTCGAC GAAGAAAGGG CCTTTGTCTG 900 AGTTCATGTC CTCCTCGGGC GCAGTGGCGC CCCTGCCGTG GACGGCTGGT CGGCCTCGGA 960 GTGGACAACA CTTCCACAGG GAGCACTATG TGGACAGGAC AGCTGGCCTT CTGGCCACCC 1020 AGTCCCCTCA GATCGCCAGC AAGGGAAGGA CAGAGACCCT GGCCTGGGTC TGTTTCAAGC 1080 CCTCTTCTGT ATGAAGGATG CTGCCCAGGC CAGCAGCGCC GCCCACCTCT GGTGCCCACC 1140 TTTTCCACCC TTTGCTTTCT GGTCCTTCCT GCTAAGGGTT CTCTTGGCTG CAAGCTCAAG 1200 CCTCAGTGCC ATGGCCTTTT TAGACAGTGT GGGAGACAGT TCAGAGCTCT GAGCTCTGTT 1260 GAGAAAAGAA AACTGTTTCT GCGTTTGGCA AAGGTGTGGG TTGTCAGCAG AGATCAAAGT 1320 TCTGTTCCTG 1330
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