Tag | Content |
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EnhancerAtlas ID | HS184-20755 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:115502680-115503860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:115503043-115503062 | CCCCGCCCCCAGGTGGCCA | - | 6.03 | CTCF | MA0139.1 | chr3:115503508-115503527 | TGCTGCCCCCTCGTGGCAG | - | 6.91 | EWSR1-FLI1 | MA0149.1 | chr3:115503790-115503808 | AGAAGGGAGGAAGGAAGG | + | 7.95 | RREB1 | MA0073.1 | chr3:115503002-115503022 | CCCCAACACACCCGCGCTCC | + | 6.06 | ZNF263 | MA0528.1 | chr3:115503792-115503813 | AAGGGAGGAAGGAAGGGGAAA | + | 6.05 | ZNF263 | MA0528.1 | chr3:115503788-115503809 | GGAGAAGGGAGGAAGGAAGGG | + | 6.63 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_02490 | chr3:115502337-115505239 | Astrocytes | SE_35267 | chr3:115501900-115504927 | HeLa | SE_36068 | chr3:115502074-115505190 | HMEC | SE_45917 | chr3:115502093-115510562 | Osteoblasts | SE_56616 | chr3:115502273-115505757 | u87 | SE_64915 | chr3:115502266-115504788 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I115783 | chr3 | 115502248 | 115505265 |
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Enhancer Sequence | ATTAAAATTA ATAATAGATT TACTGTAAAA ACAGAGCCTG CCTTGCGCGT AGCACTCGAT 60 AAACGCTTTT TATTATTCTG CTTGTTGACG CTGTTACCTC TCTTTTGGAG TAAAAGGGGG 120 CGGAATCGCA ACAAGACCCC AGGACCCCGT GTGCGCGCGC GTGTCGGGGG AGCTGACCTA 180 TGACAAACAT GTGCAGAGCT CTAGTACCCA GCCACGCGGA GGCTGCCGGT TGACAGAAGC 240 GTTGCCGCCC CCTGCCGCCG AGTTCACCCT GCCGTCACTG CTGGAAGCCG CACCCCTAGG 300 AAAGGCTGCA AACCCACCCT GCCCCCAACA CACCCGCGCT CCCTCTCTGC AGGCCGGCTC 360 CATCCCCGCC CCCAGGTGGC CAAGCAACAC CGCCTTCTAG CTTCCTCCCG ACCGGGCGGC 420 GCCTGCAGCT GCCTGGGGAA GGAGCCCCGC AGCAGCGCGA GCGGGTGGGC GGGGGGTGCG 480 CGGGCCGCAG GGCAGGAGGG AGGGCGCAGG TAGGCGGGCG GGGAGAAGCT AGGCGGCCGG 540 GCCGAGCGGT CGCGCCCAGC CCTGCCTCTC TCCCTTCTCG ACTCACAGGC GGCCTGACTC 600 ACTCCTTTGT TTCTGGAAAA GATCTATCTG TACTAGCCCG AGGCGGAATT CACCCCGCCC 660 GCACTCATCA GAAATCGTTT GCTTATTCTC TGCGCCCCTC CGTGCTCGCC TGGGACGCGG 720 GCGGAATCCT GACGCAGGCT GTCAGCCGCG GTGACGGGTG ACACCGGGTG AGCAGCCGTC 780 CGCGCCGCCT TCCCTGCGCC GACGGGCAGC GCGGCGTTCG GCGCGCACTG CTGCCCCCTC 840 GTGGCAGGAG CAAGCATCGC AGCAGCGCCG ACACCACCGC CCACCTGCAG CCCGGGGAGC 900 GTCACTTCTG GGTGTTTTTC AAAGGGAGCA TTTTTACAGC TCCATTCAAC TGCTGGGATT 960 AGGAGATGTG GCTCCCAGGT TGATTACTAA TGAATGAGAA GGGGTGTGGT CTGTGCGTGT 1020 ATGTTCTTGT GTGCGTGTAC GCGTGTGAGA GAGAGAGAGG GAAGGGGGGA GAACAACTGT 1080 AAGAGCATGT TTGTGGTGAC AGGATAATGG AGAAGGGAGG AAGGAAGGGG AAAAATGAAA 1140 GAGATTAAAA AGCAAGAGAG GCAAAGTGAC AGTGACGAGG 1180
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