Tag | Content |
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EnhancerAtlas ID | HS122-08868 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr21:38089770-38092120 |
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) |
HSF1 | MA0486.2 | chr21:38091109-38091122 | TTCTAGAACATTC | + | 7.52 | Nfe2l2 | MA0150.2 | chr21:38090440-38090455 | CAAGATGACTTAGCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr21:38089966-38089981 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I036718 | chr21 | 38090908 | 38092610 |
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Enhancer Sequence | CAGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGTGGTG CGATGTCGGC TTACTGCAAA 60 CTGCGCCTCC CGGGTTCAGA CGATTCTCCT GCCTCGGCTT CCCTTGTAGC TGGGATCACA 120 GCCGCATGCC ACCACGCCCG GCTAATTTTT GTATTTTTAG TATGACATGA TTTCACCACG 180 TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCC GCCTGCCTCG GCCTACCAAA 240 GTGTCAATAT ATATTTTCTT AAGCCAACTC TCTTAGTTTT TAGCTTCTGC CACTCCGCAC 300 CTGGACAGGC CTTCCCAGGG CATAGTCATT GCCACCCTGA GGAAAAAAGG AAATGGTCCT 360 GTCCCAAATG GCTGGCTTAC CTGTTGCCAG TTTATTTAAA CTTTTTAAGG ATTAACAGGA 420 ATGACTCGAA AGAAGAATAT TTAGTTTTAT TATTTTTCTT AAATGAAATC CTGTAATAAA 480 CTTTTCAGGG AGGCGAATGT CCGTCTGGGA GATCTGTTGA GAAAGTGCCA GGCTTGGGAA 540 GTGGGTGTTA AGTAGAGGGT AGGGAGGATT CCTCTAATAG GATTCTCTCT GTTGCTCTGT 600 TTGCATAATA TTGGAAGGAA ACATTCCATG AATAATGTAA AACATAGAAC TGTGAGAGCC 660 GTTTTAGGGA CAAGATGACT TAGCAGGCCA GAAGTGTAAC TTATTCTGAA TAAGAAAGCA 720 ACTCGCTCTT CTTAACAAAT TGGAAGAACT GGCTCAGAGG AGTGCGATAA ATCACTTCAC 780 CCCTCCACGA CCCCTTGGTC CCAAGTAAAA GCTGATGGCC TAGATGCTAA TCTGGAACTG 840 CAACTCCCAG AACTTCTCCA TTAAGCAGCT GGCTGGGTTG TCCTGTTGCG TGAGGTGGCA 900 CCGTCAGGAT GGCCACTTTG CAGATAATCA TGTTGTCTCT CCTCTGATGG AGAGCCACAG 960 GCTCCCAGCG ACACCTGCAG CAAGACACAC CTAAAAATAA CAAGGGGGTG GCTCGGGACA 1020 AGACACACCA TGAGCCTCCT TTTGTTATCT TGAGTTACCC TCTCTCCTTC CGGCAGGGTC 1080 AAGAAGGAAT TCTCCAGACC TACCCAAGAT CCTTCGCCAC CCAAGGACGG TTTCCCACAT 1140 GCTTTGAGTT TCTTCTCAGG CTGGGCACTG GGACTCCCCT TGGTGGTGGA GGAAGTCCTA 1200 CCACTGCCCC TGGGCCTCCC CTGAACAATG CTGGGGTTCA CCGACTCACT GTCCTTGTCT 1260 GCCACCCTCA GCACTATTGA TTATAGCTCT AAAAATAGGA TCCACCCACC ACTGCTCAGA 1320 AGGCTGCTCT GCTAGTCATT TCTAGAACAT TCTGTGCCAC TGTCCATCTT AAGGTGGGTG 1380 GGGGCCCAGG TGTTGAGACT CTATCATATC CTCTCCTGGT GCTTATGTTT GAGAGAACAT 1440 TCGAAAGATT CTCAAGTTCG GGAATTTGGG CCTCCAGGGA CCTCTGTGTA AAAATTGTAA 1500 CTATGATGGG TATTTTCCTG GGGCCATCCA TTCCTGCAAA GTGACATGGA TGTGCTGTCC 1560 TCTGTGGGCT GTGTCTGGAA ATAGGTAGCG TCGGACTGTT GAGGCAGCAA CCCCAGGACA 1620 TAATCCCCAT ATAACGTGGC TCTCTGGAGC AGGCCCAGAC CCTCCCGCAG GGCACGCACA 1680 GCCCCAGCCA CACCCCTGGG CGGGAGCCAC AGAATTAGCA CAGTCATCTC GGACTGGGAG 1740 GGCCAGAGAC TCATTGCTGG TAATGTGAGA GAGGCCTGGC AGCGCCTGAG GGGCACAGCT 1800 CAGAGTCGAC GAAGAAAGGG CCTTTGTCTG AGTTCATGTC CTCCTCGGGC GCAGTGGCGC 1860 CCCTGCCGTG GACGGCTGGT CGGCCTCGGA GTGGACAACA CTTCCACAGG GAGCACTATG 1920 TGGACAGGAC AGCTGGCCTT CTGGCCACCC AGTCCCCTCA GATCGCCAGC AAGGGAAGGA 1980 CAGAGACCCT GGCCTGGGTC TGTTTCAAGC CCTCTTCTGT ATGAAGGATG CTGCCCAGGC 2040 CAGCAGCGCC GCCCACCTCT GGTGCCCACC TTTTCCACCC TTTGCTTTCT GGTCCTTCCT 2100 GCTAAGGGTT CTCTTGGCTG CAAGCTCAAG CCTCAGTGCC ATGGCCTTTT TAGACAGTGT 2160 GGGAGACAGT TCAGAGCTCT GAGCTCTGTT GAGAAAAGAA AACTGTTTCT GCGTTTGGCA 2220 AAGGTGTGGG TTGTCAGCAG AGATCAAAGT TCTGTTCCTG GCAGGGTGAG CACCTGTGAC 2280 ACACCTTGCC CCTCCCCCTG CGCCAATCCC AGAGAGGCGG TGGCATTTCT GACCCTTCCC 2340 TTCCACGGCA 2350
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