Tag | Content |
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EnhancerAtlas ID | HS184-32035 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chrX:16680150-16681520 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chrX:16680625-16680642 | AGGGTCATGATGACCTA | - | 6.72 | ESR1 | MA0112.3 | chrX:16680625-16680642 | AGGGTCATGATGACCTA | + | 6.82 | ESR2 | MA0258.2 | chrX:16680626-16680641 | GGGTCATGATGACCT | - | 6.3 | Esrra | MA0592.2 | chrX:16680222-16680233 | TTCAAGGTCAA | + | 6.14 | Nr5a2 | MA0505.1 | chrX:16680219-16680234 | AAATTCAAGGTCAAG | + | 6.3 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAATATTCAA AATATAAAGT CCAAAGTGCT GTGAACTACA CTACAGATGT ACTGGAGAGA 60 TCTGAAGCCA AATTCAAGGT CAAGGATGTC AGCAGCAGCC ATGTGATTGA TATAGGGTTA 120 GAATGTAAGT CAGCAACAGC TACGCTCTTG GTTATGTACC ATCTAGAAGG CAGCTGAGAC 180 TACTTTGAAG CAGGGCAAAA AACCAGAGTT GCTATAGAAC CCTAAGTATT CTGCAAAGTC 240 CCAGAGCCTT CAATTTCACC TTGTGGATTA AGCAGAGAAA TGACACAATA AAATAAATTT 300 TACTCATTCT CTCCTGGGCA CTCTGAGACG CAGAAAGAGT CTACCTTAAC CCTTAGGGAA 360 AAATCTGTTT CTCTTTTTAT GTGTATAACA GACACTTTCT CTTGGAACTG TTCTGGATGC 420 CAGTGTCTCT ATTGATTTCA TCAACAGCCA TAGCACTAAT CATGCATGCC AAAGGAGGGT 480 CATGATGACC TATGAAGAGA TCTTAGGAGT AAATATTCCC TATAGAAGGC TCCTGGTTTC 540 CAAACTGTTT ACTTTCCTAG CTAGAACAGC CAGAATGACC AGTCCCCACA AAGTAACTGT 600 TATTTGCTCA AGCTTAAGTA ACTCTGCAGG CTTCATGGTG CTTGCTGCCT TATGATTCTA 660 TCTCCTTAGT CTTTTTTTTT TTTTTTTTAA TAAGACTTCT CACATCGATA CAAGTGCTAG 720 CTCTTAAGGC TATTTTTCTC CAACAAACAT TGCAGGCCAT AAAGACGTTC AATAGCAATT 780 AGCTTTTATT GTTCTCATCT CACTTATGTG TATAGGAGCC ATCAAAATGT AAAATGCACA 840 CATCCTCTGA CTTAGCAACT CCCCTTCTAG GAATCTATCC CTGCAGATGT GTTCGCGCGT 900 GGGTGCAAGG ATATATGTAC ATGGATACTA ATTTGCAGCA TAAATTAAAG CAGCAAAATA 960 ATGGACACAA ACTAAATATG AGACTGGTTA AATAAATAAG GATGCAGCCA TATAGCATAC 1020 AGCAGAGCAA GCACACCGAA GACATCCCTG CACATTGATG TGGAATGATC AGTATATAAA 1080 GCAAGGTGGG AACAGTGTCT GGAGCATGCT ACAAAGTTGT TTTGTTTGGT TTTGTTTTGA 1140 GACAGGGTCT CGCTCTGTCA CCCAGGCTGG AATGCAGCGG CGTGATCACA GCTCACTGCA 1200 GCTCAACCCC TGGGGCTCAA GTGATCCTCC CCCTCAGCCT CCCGAGTAGC TAGGACTATA 1260 GGTGCATGCC ACCATGCCCA GGTAATTTTA TTTATTTATT GTAGAGGCAA GGTGTAACTA 1320 TGTTGCCCAG GCTGCTCTCA AACTCCAAGA CTCAAGCAGT CCTCCCGCCT 1370
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