Tag | Content |
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EnhancerAtlas ID | HS184-28524 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:105280020-105281880 |
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) |
ESR1 | MA0112.3 | chr7:105280531-105280548 | CATGTCAGAGTGACCTG | - | 6.03 | ESR1 | MA0112.3 | chr7:105280531-105280548 | CATGTCAGAGTGACCTG | + | 6.15 | ESR2 | MA0258.2 | chr7:105280532-105280547 | ATGTCAGAGTGACCT | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33206 | chr7:105279795-105280998 | H1 | SE_68778 | chr7:105278057-105283234 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I105638 | chr7 | 105278053 | 105282263 |
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Enhancer Sequence | TTTAAGAAAC AAACAAAAAA TATAAGAAAA AAGGAGACTA AATAGGATTT GGCATTAAGA 60 CTACATTTTT TAAAAAATGC ACATTTGCAC CAACAAGTGA GACATTGTCA GGCAATCTGT 120 TTTTTGTTTT TTTGTGTTTT GTTTTCTCAA CCAGCTGCTA AAAGTCTTCC AGAACCGCTC 180 GGGGAAAATG GTGCTCCCCT CTGAACCCAG AGTTCCCAAG TCTAGCTTCG GCAGCACCGC 240 CGAACGCAGC ACAAGGCTCG GGGAATAGGG CGGGAGCAGG CACCGAAGGG AAGGAGAGGA 300 GCCGTGCTGC TCTTAATGCT CTTAACGCTT TATTTTACTT GCAATGGTTC CACAGGTCCT 360 TGGCATTTGG GCATAGCTGG CTGCAGACCA GGGAGAGCCA CCTGAGACCC AACGACCCCT 420 TTCCTGGGCT GCTCCAAGAG TACAGACACC CTGACTCCAG CTCCTGCCTT CCTGCTAGTT 480 TTAGCCATGT AAATGGGAGA TTACTCCTTG ACATGTCAGA GTGACCTGCC TCTCTCATGC 540 TTGACAAAGC TCTCGGCGCA GGCTTTGCAC ACAGCCTTGC TGACCACAAA CACCATTTAC 600 CTGATTGAGG GGCACTCTAG CAGTGTTACA GGCAGGGGCA GGGGAGAAGG CTGAACTTGA 660 AGGTGCAGAG AGGGCAGGGG CCTGCTAATC TCACAGCTGC TCCCCGCCCC CACTGCCCTG 720 GGTCTGATGC TTCACGTGGG AATAAAACGG GGCAGGCTGC CCCACCAGGA TGAAGGATGT 780 CTGTGCGGAG AGGCCAGGCT TCCCCAGCTC CTGCCTTCCA GTTGACTGTG GACAGCTTGT 840 GCGGAGGTTA CTTCTAAGGA GCCTGCTCTT TCTATACCCA TCTTGGGTCC TTCACCCCTG 900 CCAGGAAGAC AATCATGCTG TCCTCACCTT AAAAATGAGG GGATGTGAGG TGATCTCTTT 960 TTTTCATTTT TATTTTTTGA GACAGGGTCT CGCTCCGTTA CCCAGGCTGA AGTGCAGTGG 1020 TGGGATCACA AGGCTCACTG CAGCCTCGAC CTCCTGGGCT CAAGCCTCAA CCTCCTGAGT 1080 AGCTGGAACT AGAGGCATGC ACCACCACAC CTGCCTGATT TTGTTATTTT TTGTAGATAC 1140 AGGGTCTCAC TATATTGCCC AGGGTAGGTG ATCTCTTAAG GATCTTTTGG GCTTTAAAAT 1200 TCCACCTCTT GGATGGCCTG TGCCGTTTCT GGAAGGCACC GAGCAAACAC ATAAGTCCTG 1260 CAGAGCAGGA ATGACACAGC CCTCTGGGCA TGTGGGTAGA CTGGCAGCAG TGTTGCTGGT 1320 GGTAGAGGGT GTACAGAAAT TGGTGGTATC TCCTTAAGAC CCTTGAATGG CTGCAAACTC 1380 AAAAAAGGTT CCTAGCTGGA AAACTGTCTG AAATTGGTGG AGTAAACTCC GAGCATATAA 1440 CAATGCTCAG ATTATACCAT AATAAATGAA TGTATTCTAT TTTCAAAAGC TTTGAGGGTC 1500 ATGGGGAGGT TGCAATGGTG TTACTGATGA TATGCACAAG AAAACTACTC TATACCCAAG 1560 ACAGATTCCC TGGCTGGTTA CCAAAATGCC TCCCCCCTTT TTTTGCTTTT TGTCTGCCTT 1620 TTCTCTCTCT CTCTCTCTCT CTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TAGCTTCACT 1680 TAGAAAAAAA ACCTGCTAGG CCTGGAGATG CTGGTTTGCT CGGAGCCCTC TCTGGCCAGG 1740 CTGCCTGGTG TGGTGTTTTT TTTTTGGGTC TGTCAGAGTC AGGCCTGTGC CTGGTCCCAC 1800 ACCAGCGCCT CATGTCGACC TGGAGCTGAG CAGGCTGTTG GCTGAGGGTA GGAGCTGGCT 1860
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