Tag | Content |
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EnhancerAtlas ID | HS196-12280 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr17:81057220-81058400 |
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) |
PLAG1 | MA0163.1 | chr17:81057741-81057755 | GGGCCCCACGGGGG | + | 6.01 | SOX10 | MA0442.2 | chr17:81057976-81057987 | AAAACAAAGAA | + | 6.62 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_01998 | chr17:81052811-81058405 | Aorta | SE_23159 | chr17:81056623-81058473 | Colon_Crypt_1 | SE_23811 | chr17:81057276-81057907 | Colon_Crypt_2 | SE_23811 | chr17:81057996-81058475 | Colon_Crypt_2 | SE_24692 | chr17:81055617-81058556 | Colon_Crypt_3 | SE_26841 | chr17:81056992-81058441 | Esophagus | SE_28661 | chr17:81055584-81057437 | Fetal_Intestine_Large | SE_32097 | chr17:81057299-81058039 | Gastric | SE_35080 | chr17:81057198-81058414 | HeLa | SE_44287 | chr17:81055990-81057897 | NHDF-Ad | SE_47794 | chr17:81057395-81058367 | Pancreas |
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Enhancer Sequence | CAGGCCCCAT GCCTCCCCTC CCCAGTGCCC CCTACCCCCA GGTCTTCCCT CTAGGACATC 60 AGCCTGGGCT GTGGGTCTTG GTCTCCCACA GAGACTGAGT CCTGGGAGAA GGGCAGAGCC 120 TTGGTTCCCA GTGCAGCCCC TGTGCCAGCC TGCAGTGGGC ACCGGTTCAG CCGGTGCACA 180 CTGGGTCCTG CCCCCACCTG AGGAGCGGCC TGGGGCCTGA TCAGCCCTGC TGGTGTCTGG 240 CCTGCAGCCA GCACCGGCTC TGCTATTCAC ACTTGGTTAC AGGTGGGTGC CCATCCCAGC 300 AGCCTCGGAG CAGAGTGGGT CGGGCTCCGG AGGTGGGGGC GGCCACTAAC AGCAGGAGGT 360 CGTGGCAGTG CGGCTATGGC AGGGGTTCTG AGGGGCGGAA GCCAGGGGCG GGACGTGGGG 420 ACGCAGACCT GCAGGGAGGA CGCCGGCTCA CCCAGCAGGG AGGGGATGGC CGCCCAGGGA 480 CCCCCAGCCT GCCCGCTCTG CTTCCCCGAC CGCCGGGGCA GGGGCCCCAC GGGGGACGCC 540 AGGGAACGTG AGGAATCCGG AGTCAACACT GGGCCACTGT GTGCTGCCAG CCGGGCGGGC 600 CGTGATTTAT AAAAACAGCG GAGGCTTGGC TGGTGTCGGG GCGGTGAGGT CACGGCGGCC 660 GGGGGCTCTG GAATTTCTTC AGAAGAATTT TGCTTACCAA GCCACATACT TTTCTAGCCA 720 TCAGTTTGAT CAGAGGCAAG ATGAAAAATA TGCTAAAAAA CAAAGAAACA AAAATACACC 780 CCGGGGGGCT CCGGTGAGGG GGAGGGGCGC TGCGGGAGGG GTGGAGGGCC CAGGGAAGGG 840 TGAGGGGCCG GGAGCCACTC TGCCCGGCAC TCTCCGCCCA GAAACAGCCC AACGCCCCTT 900 TCTTTCCCCT TTTAGCACTG CTGAGCTGGA CTAAAATGCC CAACAAGGAA CTTTACTAAA 960 AACTGAGGCA AGAAAGAAAA CACACATGAC ATAAAAATAG TCAAGGGCAC ATTCTTGATG 1020 GTAGATAACT GGTCTCTGGC CACAGCGGCT GCCAGGTTGG GTGTCGGCCG GCGGGTCTGC 1080 CAGTCCCACT CATAGGCACT GCACTTCCCT GGGCCGGACA GGGGGTGTGG CGGGTCTGTG 1140 GGAGGGGGAC AAGGTTGGCA GGACCGTGAG GGGGGTGGCG 1180
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