Tag | Content |
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EnhancerAtlas ID | HS184-12862 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:85854640-85855850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:85855165-85855184 | TGAGCACCAGGTGGCGCTA | + | 6.93 | RELA | MA0107.1 | chr16:85855374-85855384 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr16:85855064-85855084 | CCACACATCAACCCCTCCCC | + | 6.78 | ZEB1 | MA0103.3 | chr16:85855094-85855105 | CCCACCTGCCC | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH16I085821 | chr16 | 85854841 | 85854990 | GH16I085822 | chr16 | 85855121 | 85855490 |
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Enhancer Sequence | ACAAAACAAA ACAAAACAAA ACAAAACAAA ACAAAACAAA ACACCATGTT GGCCCAAGGC 60 CAGCGTGTCT CAGTGAAGGC TGCACGTTAG AATCACCTGG GCGACTGTTT CAAGGCGCCA 120 CCCCAGACAC AGCTACAGTT TCAAGTTCCC CTCAGGTGAT TCTAATGCAG GTTCAAGCCA 180 CTGCATGCAT CCCACGTTGC GTGATCACGA AAGTCACCTG GGAAATTGGT TGAAAACACC 240 AATCTCTTGG CTCCAACCCA GAGCTACTTA ATCAGAATCT CCAGGGGGAA CAGATCTGAG 300 CTTAACAGCC CACAGGTGAA CACCTTGAGG CCAAAGGAAC CCATTCATAA AGGGGTGGGG 360 GCCCAGCTTC TTCTGAAGAA GGCTGGCGGG AGTTGGGGGG AGGTCCGCAA TGCAAGGTTG 420 CCCTCCACAC ATCAACCCCT CCCCCAGGAC TGTACCCACC TGCCCGCATT TGAATCTGGG 480 CCACCTTCCC GGCCCGCGGC GCGGAGTTGG CGGTCATATC CCGCGTGAGC ACCAGGTGGC 540 GCTAGGGCCC CGCGCTTGTC CTGGAGCCCC GGCAGCTGCT GCGCTTCCCC CAATTAATCT 600 CTCTTCTGAA ACCATAGCTG CTGAGAAGCT GCAGAGGGAG CCTGCGCCGT CTGGATTACG 660 TGGCAGTGAC CCGATGGTCC TGCCACACAG GTCAAGTTCC TTTAAAAGTC TTGTCCTTGA 720 TCTCGAAAAT CCATGGGAAT TTCCCATTTT GCTCCATGGT GCGCTGCTGT GTTTGTTTTA 780 ACACAGAAAT AAGTATTTCC ATAAATTCCA CAAGACACAG CTCCCAAAGA TGCACCTGCT 840 TTTACAGGTT TCTTGGCCCT GCACCCCCTC GGAGGTGAAT GGAGCCTCCC TGGTGTGAGA 900 AGTGCAATCC ACGTGGTTGG GGTGTAGGTC TCCCTCCTGA TCTAAGAGGG AGAAAATGAG 960 ATGGGTGGGC ACTCCCCACA CCTGTTTCTT CATCTTTGCC ACACTTCTGC TAGGGGAAGG 1020 ACAGGGCGTC CATCCTCAGG GCCAAGCCAG AGCATTCTCA TCTGCTCAAT AAATTTCAAT 1080 TTACTTCTGA GCACGTGTCG TTATCAAATT ATCTGTGTGG CGCTTTCCAC TCCCACTCTT 1140 CTGAAGATGA GCATGTGTAA CAGAGCGGAA CACATCTGGG CAGCCGAGGA AAGGCCTCAC 1200 TTTAGGAACC 1210
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