Tag | Content |
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EnhancerAtlas ID | HS187-15589 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:61347250-61348700 |
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) |
FOSL2 | MA0478.1 | chr20:61347596-61347607 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr20:61347596-61347607 | GGATGACTCAG | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34310 | chr20:61332706-61349814 | HCT-116 | SE_49961 | chr20:61345737-61349280 | RPMI-8402 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I062715 | chr20 | 61347271 | 61348251 |
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Enhancer Sequence | TGGGCTGAGC AGGGCCCGAG AGGACGTCCG ACCTGTGCAC GAACCAGAGG CTGCCTTCGT 60 TTTTCTCAAT CAAATCTCAC GTGGTGATCT AGTAGTTTGT ATTAAGAGAA GAAAGAAGCT 120 TTTCTTTATT TTTGATTCAT GGTGAAACAC ACATCACTTA AAATGTGCTG TTTTACCATC 180 TGGAAGGGCA CAGTTGAGCG GCGTGAAGCA CGTTCACATT GCTGTGCAAC CGTCGCCACC 240 ATCCACCTCC AGAACCTTCT CTCTCCCCAG ACTGAAACTC TGTCCCCATT AAACCCTGAC 300 CCCCAGCGCC TGGTAACCTC TTTTCTGCTT TCTGGCTCGG TGAGGTGGAT GACTCAGACT 360 GGCAGAATCT CAGGCCTCCC CTGGGTCTTC TCTAAGATGC AGGTTCTTGA AGGCAGGCTT 420 GCTGCTGAAA GACGCCAGAC TCCAAGGCCC TGGGTGATTC CAAGCACTTG AGGTTCTGGA 480 CAACGCTGAG CCGTTGGGAC AGGAGGAAGG TCGGAGGAGG GGTGGGGTGG CCATAGGGGC 540 GCTGGGAACT CTGGGGTGAC GGAAATGTTC TGTATCTTCG TTGTGGATCA TAGCTCGTGG 600 TTTCAGCGCG TTAGTCCCGC CTCCGTGAGT CTGTGTTGGT TGTGGTTCAA AGCTCGTGGG 660 GCTGTAGACT GAGGGGTGGA TTTCAGCGCG TGTTAGTCCT GCCTCCGTGA GTCTGTGAAA 720 AACAACAGCA GCAGAGAGTG ACCGAGCTGC CGTCCGCTCA AGGCTGTTTC GGGTGGCCAG 780 GTCCTCCCTC CTGTGGGCCT GTGTGCACTC AAGATCGTCC TCCCCTGGAC GGCCATGAAG 840 GGCTGTGAAG AGCATGAGCC CCCATCCCGG CAGCCCCTCG CTCCCTGACC AGGCTGCTGC 900 CTGCACGAGG CTAGCTCTGC AAGGGGGGCA CGGAGGGGAA TAGAGATCCT GGTTCTTGGC 960 GCTTGGTGGG GATGGTGTTA CTGAGGTCAC AGCCATGGGG TCTGCCTGTC TCAGAGACCC 1020 CCACTGTTCC CCCGCCATGC CCTGGAGTTT GACCTTGCCA TCGCCAGTGA AGGCGCAGTG 1080 GCCAAGGGGC TGTCCCCGTC CATGTGTCAC CCCAAGGGGA ATGCACAGCT CCGGAGGGGG 1140 ACCACCGGGC TCTGCAGCGT CAATGAAGAA ACTGAGGCCC AGAGCGGGGC AAGGCGCCTG 1200 CCCCACCCTG GTGCCCACTG CTCTTCCCAA AAGCATTGCC AGTGGGGCAC CACCCACCCC 1260 AGGAGGGCAA GGTGAGAGCC CTGGGTCTGG AGTGCCACGT GGACCTGGCA CAGGTTGGAG 1320 AGGGGAGGTG CCCAGCATGC TGACCCACCC GAAGCCACCC GTGCCTACTT TGGGATTTTA 1380 CATCCCTGTG CACCTGTGGG GGCTGTGTCC TACATACCCA GGGCTGGCTC CTGAAGGCAG 1440 TCAGGGAAGC 1450
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