Tag | Content |
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EnhancerAtlas ID | HS184-31408 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:116881810-116883030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:116882845-116882863 | CATTCCTTCATTCCTTTA | - | 6.04 | EWSR1-FLI1 | MA0149.1 | chr9:116882841-116882859 | TCTTCATTCCTTCATTCC | - | 6.78 | KLF5 | MA0599.1 | chr9:116882822-116882832 | GGGGCGGGGC | - | 6.02 | RREB1 | MA0073.1 | chr9:116882165-116882185 | GGTGGGGGGGTGGGGAGGGT | - | 6.21 | RREB1 | MA0073.1 | chr9:116882147-116882167 | AGTTGGTGGCTGGGTGGGGG | - | 6.26 | RREB1 | MA0073.1 | chr9:116882157-116882177 | TGGGTGGGGGTGGGGGGGTG | - | 6.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 116882000 | 116882121 | chr9 | 116882242 | 116882800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I114117 | chr9 | 116879643 | 116882763 |
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Enhancer Sequence | TTCTTTTTCT GTTCCAGCCC ACAGTGCAAG GGTAGAGACT CCAGGAAGAC TGTCTCCTTT 60 ACACTTGGAC CCTAGAAGGC TGGTCTGTGC TGAGGGTCAT AAGAAGCTGG TAAATTGAGA 120 ATCAGGGGTT TCTGCCACCC ATGGCATTAG GCGGCAGAGA TACATGTGTG TGTGAACTAT 180 CACGAGGGTC TGTCAAACAG GCCCTGCAGG AAGCCCAGGC AAGCCCGGGT GACCTTTCAT 240 CCTTTCCCCC AGAGAGCTGC ACAGAATACA CCTCTGTCAG ACAAGGGTTA ACCTGGGTGG 300 GAGGGAATAT TTACACTGGC TTTTCTTTGC AAATAAAAGT TGGTGGCTGG GTGGGGGTGG 360 GGGGGTGGGG AGGGTCGGGG GGTGTCCCAT AAAACAAAAA GGAAATAATC TATGCAAAAA 420 CTAAATGGAA ACGTGTTTTA AAAGACTCTA CCAAGAGCTT GCTGAGTGAC CCTGAACAGT 480 GGGGACTTAG GGAAAAGTTG ACAGCATCCC CTTTAAGAAG AAGTGGTGTA GCATAGGTAG 540 GGCCATGAGC ACAGGCTTTG GGGCTCACAG ACCGAGGTTA GAATGTGGGC TCTGCTCTTC 600 TCTGGCTATG TGACCTTGAG CAAATCGTGG ACCTCTCTGG GCTTCCATTT CTTTGATTTG 660 TACAAGAAAA GAGAAGAGAG GGTTAAAGTA TGTGAAGGTC CCTGGCACTT CATGGATGCT 720 CATTAAATGT CAATTTCCTT TCCTTTCTGG GCCTCTTGGC AGGTCGAGGG GAAGTGTCTG 780 ACAGGTCTCA CCAGCCAGAC TGGAGAGAGA CACAGCTCTG CAGGTCTCAG TGCCTGCACA 840 CCAGCTCAGT AGCCTGATGC TGACTATGCC CCTAGAGCCC TTTACAGTTT GTAAGGCATT 900 CACCTACTTG CCGTTAAAGC CTCCCAAGAA TCCCATAAGG TGGTCATGGC AGCATTTACT 960 ACCTTATGGT GCTGTGACTG GGAAAGGGTA AGGGACAAGA ACCCAGTGCT CTGGGGCGGG 1020 GCCCAAGTCT GTCTTCATTC CTTCATTCCT TTAGCAAATA TTGATTGAGG ACTTGTTATG 1080 TCCAGGCACT ATGCCAAGCA TGGGAGATAC ATAATGAATA AAAATCGACA CAGATGGGTG 1140 GTTGATGGAT GGGTGGATGG GTGGATGCTG GTCAGATTAT GGGTGGGTAG ATGGATAGAT 1200 AGATGGATGA TGAATGGATG 1220
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