Tag | Content |
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EnhancerAtlas ID | HS012-12018 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:120536960-120539060 |
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) |
EWSR1-FLI1 | MA0149.1 | chr12:120537587-120537605 | GGAAGGCCAGAAGGAAGG | + | 6.52 | KLF5 | MA0599.1 | chr12:120537743-120537753 | GCCCCGCCCC | + | 6.02 | ZEB1 | MA0103.3 | chr12:120537019-120537030 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27057 | chr12:120537449-120541185 | Esophagus | SE_31982 | chr12:120538202-120540645 | Gastric | SE_41982 | chr12:120537882-120541422 | LNCaP | SE_68937 | chr12:120538843-120541016 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I120099 | chr12 | 120536948 | 120540903 |
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Enhancer Sequence | GCAGGGCCAG AGTGTGCGGC AGCATGTCAA CCCCGACAGG AGTCACCCCC TTGCCGGGAC 60 CCACCTGCCC ACGTCAGGAC ACTGACCCGG AAAAGGTGAG GGTGGCCCTG GAGCCTGGGC 120 TCTCACTCAG CCTCGGCAGA TGCCCCCGAG CCACAACAGG CCAGCAGGAG AGGCTACTGC 180 GGCAGCACTG ACTCCCCCTG CCCGCCCGGG GCACCAACAG GGCGGGAGGG CCAGCCCCTG 240 GGCAGCAGAG CAGGTCTGAG GAGTCACCTC CTGCTGTTCA GAGTCTGCTG CAGGCTTGAA 300 ACATCTTTGA AGTTCTTGCT TTATTTTGGG AAATCAGGCA GTTTTTGTAT TTGACATCAT 360 GTTATCACTG TCTTTGAACA TTCAAAAAAA TATTTGCTCC TCAAACCTGT TTTAGAGAAC 420 CTTTCCAAGA AGCCACACCA TCATGACGCC CTGGCAAAGT CTGTGCCCCT CCCCTGGGGC 480 AGGTAGGCAC CTCCCTTCCT GCTACTCTTG GCTCATCTGT GCAGGTGGCA GGAAAAGCAT 540 GGAAGCCACA CAAGCATCCA GGGATGGCTG GGGAGAGGGC GCCCAGCAAA GCCATCACCC 600 CAAACATGCA GAGCCCAGGG CCAGCCAGGA AGGCCAGAAG GAAGGGGAGG CCCAACTCTC 660 CTCTCCAGAC CCCATGTCCC CATTCATCCC AGTGGCACAG GACGACATCA ATCCCCGGAG 720 GAGGAGGGGG ACCACAGCCT CCGCTTCCCC GAGAGCTGTC GAAGAGCCGG AGGCCAGGCG 780 GCAGCCCCGC CCCACACTGT GCAATCAGCC AGAGCTGTCC CTCTGTCCCC TCTCCCCAAA 840 GCCGCAGGGA CCTCCACCCC AGGGCTCCTC AGGACAGCAC ACAGACAAAC CATGAGTGGA 900 CAGGCCGCTT CCTCCCGGCT TTCTGGCTGC CACCTGCCCC AGCCCTAATT ACCTCCACCC 960 CCATGAGGTT CATGGGGACA GCCCAAGCCC CAGTTCAGGA ACAGCCCAAG TCAGCGCAGG 1020 CTGAGCAAGA ATGGGGCAGC CAGGCTGACT TGTGGCTGCA GCTCCATTCC TGTCCACCTG 1080 CCCATCAGCT CTCTGGCCAA TGCTTCACAT CTGAGGCCCG ATCTAAGGAC AAAGACCAAC 1140 CCTGGCTCCA TCTCTGAAAG GCTGGCCCTT GGGAAGGTGC CTGCATTCAC CCTGCCACAC 1200 CTTGCAGCTT CAACAGTTAT AGCACACAGG TGGCTAGTCC TTAACTGGGG TGGTCATGAG 1260 GAAGAAAGGA GCTAAGCATT ACCCCAAGGC GGGGGAGCAG TAAACAGTCA GTATGCGTTC 1320 TTCAGCATCA TCAATGTGCC TTCAAGGACA ATCTGTGGTC CCAGACAGAG GTGGTGGAAG 1380 GAAACCAACA GGCAGCTTAG GGGCAGCCCT GAGCATCTTC CCTGATGCTG CAGAGCCAGA 1440 GCTCCTGCCC AGCCCTGGGA CAAAGCCCAA CCTGCCCCTG CCACCGCCCC TGCCCCATCC 1500 TTGCTCCATC CTCAACACGA CCGCTGGGAT CTCTTCCCAG GGCTTCATTC TGCCCACAGC 1560 TTTGCTTCCA GGGCAGCGTC GCTCCTTGGC TTCGGGGTAG CTGTGACGAT CAAGCTCTCT 1620 TGGCACTGGG CCCAAGAACT AGCTCTGGCC TTGGCAGCTG CTGCTGAGAG CGCCGGGTCA 1680 GCACATGGCA TGGTGTGTCA GACGCCTTCC AGAGCGAGGG CGCGCCGGAG CCACAGGAAC 1740 AGGCGACTGT CCCCTGCCAG CAGAGGAAGC CCAAGGAGCG GATGGCTCTG CAGACTCTCC 1800 TTTGCTGAAG ATGATCAGAG ATGCCAAGAA ACGCCTGCAG CCATGGCCCC GGCGCACAGC 1860 CCCCGCGGCT CCCTGGGCGC CTCTGCCTCA TCCGGGGCCC AGGAAAGGGG CTTTATCTGA 1920 GAGCAGAGAA TTTGTCTGGG GATGAAGTCA GGGGCTCAGA GCTCTGGCTA GGAGGAACCG 1980 GAGCACCGAC GTTTCCCATG GCCACCAGGA ATCACCTTCA CTCACAGGGA CTCTGCTCTA 2040 GGCCAGGCAC AGAGCTGGGG GCTTGGTATC CATTACCTTA TTAATGTCTG CAGCCACCTG 2100
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