Tag | Content |
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EnhancerAtlas ID | HS098-27717 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:33772570-33774240 |
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) |
Arntl | MA0603.1 | chr19:33772638-33772648 | GGTCACGTGC | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_23808 | chr19:33771609-33772766 | Colon_Crypt_2 | SE_24807 | chr19:33771482-33773235 | Colon_Crypt_3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I033282 | chr19 | 33772907 | 33773107 |
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Enhancer Sequence | CTACTGGGGA GGCAGCAGGA GCCCGGGCAG ACGGCTCATC TGAGCTCGGC CTTCTGTCAG 60 CTGACAGGGG TCACGTGCTG TCTGGGCTTG CCTGGGGCCT GAGAAATGGG GATGCGGACA 120 GCCATTGTCA GGGCTGTTGG GGAAATTCAA GGAATGGAAG AGTCAGAGGG AGTTGGGAGG 180 CCATGTCTCG GTGTGTGCGG GGGCATCGAA AGCCCTGCTG GATTTGGGGG ATCAAAGGAC 240 CGCCACGCAT CACTTGTGGG GTCTCGGGAT GATGGGGGTC AGGCCTGCTC TTTGCTGGGG 300 AGGCCAGTGG CTAGCAAGGT CTGGGGCTCA GTGAATAAGG CCACGCTTGC AGCCGCCCTT 360 GTCCCAGTGC TTGGAGAGCC ACCAGGCAGA CTTTATCTGC ATCCCTGGAA GTGACCTGAA 420 GAGACTGCCG GGCACTAGAG GGGTCCATGT GGGACCCGGA ACCCAAAGGA TCAGGTTCAC 480 CAAAGCCTGG ACTTCCCTGG AGGGCCCCTG ACCCGTCTCA GCGGCCGTCA GGCATCCGCC 540 AGCTGGGCCC TGCGGGCTGT GCTGCCCGGT GACTCCAGAG TCCTCCCACA CCCACTTGGA 600 CTGGGTCCTC CCGTGGCTCT GGCAGCCAAG GTTTGGGAAA TTAGGTGAGG GGGGCCTGGG 660 ACGAGGGTGA GGAAAGGAAC AATTTATGTT CAAAAGTCAT CTTGAAATTT TCAACATATT 720 TTTTTATTTT TCAAAACAAA AGCTCTAAAT GTTGGGGCTG GGGGGTGGCG GTGGACCTAG 780 CTTTGTGGGA AGTGAGTCAG ATGGCCATAA AATGTGTTTT TCTGAGCCGA GGGGATTATT 840 TTACATCTTG TGGCATGGAG ACGCCAGGAG GAAGCCCTCC TCCTGGTCCC TGGTGGGGCT 900 GCCTGCTGCT GGGCCTCAGC ACTGATCTCT CTTCTTGAGA TGGGGGCTCC TGCCCTTCCA 960 GGACCCCTCA TCAGCCCTCT CCCTCCCTGA CCTCACATCC CGTTCTTTTA GGCAAGAGTG 1020 AGGCTGGGAA GGTCGTGGCT TCATGGTGGG GCCTCGTACT GGCTGTGCCA TGCCAGAGAA 1080 TCTGGGTAAA GTATGCCTTG GGGACCCTCC CCAACCCCTC GTCTGATGGA TAGGCTGATG 1140 GCGGGACCAC CTCCCAGAAC AGCCACCAGC ATGAAAGGAG GGATTTGAGA ACTCATTTGC 1200 AGGCCGTCAG GGCTCGGCAA GTGGGTGCCC TCCCACCTCC AAGAACATCC TTGAGTGCAG 1260 GTGAATGAAT GAAGGGCAAA AGGGGCAACT AGGCTCTTTG GAGACCCTTC CTAAAGCCAG 1320 AGGCGCAGGG GTCCTCCCCT AATCTCCGCT ATCAACGGCA TCTTCCCTGG GACCACAGCG 1380 GGGCAGTGGT GGCTCAGGGG AAAAGTCATC TTGAAATGTT CAACATATTT TTTTATTTTT 1440 CAAAATAAAA GCTCTAAATG TTGGGGCTGG GGGTTGGCGG CGGACCTAGC TTTGTGGGAA 1500 GTGAGTCTTC CCAGGGAAGA GGACGCTGAG TCCCCACCTC AGCGACCAGA GACCTCAGAG 1560 GGGCTAGGGT CAGGGACTCC AGATGCCCAT CAGGACAGGA CCTGGTGGCT TCAGAGGCCT 1620 CAGGGTACAG GTCCCACCAC CCAAGGCAGG GACTGGGTGG GACCCGTAGG 1670
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