Tag | Content |
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EnhancerAtlas ID | HS121-20730 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr19:50103200-50104740 |
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) |
Crx | MA0467.1 | chr19:50104536-50104547 | AAGGGGATTAG | + | 6.32 | INSM1 | MA0155.1 | chr19:50103556-50103568 | TGTCTGGGGGCA | + | 6.44 | ZNF263 | MA0528.1 | chr19:50104408-50104429 | GGAGGAAGAGGAGGTGAGGAA | + | 6.96 |
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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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Enhancer Sequence | CTCTGGGCAG GTGGTCTGGG AGTAGAGCTT AAAGGTTATT ATGATCACTA GGTAACAGTT 60 GTGCAGGTTA CGCACTGTTT AAGAGACACC ATTCACATAC ATGGTGTAAG CTTGCGTGTT 120 TATGAAGGGA CTTTCCTGAT TACACAAGCA TTTTGAGGAA GGTCTATCTT TTTCTAATTC 180 ACTCAGAGGT GCTAAGTGGA CTAGGAGGGG CCCCAAGGCA GACACTGGAG AATGCAGGGA 240 GACAGGGCAG GTGATAAGTT ACAGGGACAG GACAGGGGCT ACTCAGGTTC TGAATGGTGG 300 GAGGTGTGGG AACTGAGGAG GGCTCTGAGT CAACTGTGTG TGAAGGTACA GAAAGATGTC 360 TGGGGGCAGA GAAAGACTTG GGGATGGGGG TGGGCGGTGG AAGGGAAGGC TAGGGGCATA 420 GGAAGGGTTT AGGTTGTGCT CTGGTTTTGG ACACAGTTTA AGGAGTGTAA TGTCAGAAAC 480 AGAGGCATTG GGAAATGAGA GGTGGGAGCT TACAGGAGGG CACAGAGGGG AGTGTTCAAA 540 AAAAAAAAAA AACCATGACA GGCCGGGCAT GGTGGACCAC ACCTGTAATC CTAGCACACT 600 TTGGGAGGCT GAGACAGGAG GATCGCTTGA GCCCAGGAGG TTGAGGCTGC AGTGAGCCAT 660 GATTGAGCCA CTGTACTCCA GCCTGGGTGA CAGAGCAAGA CCCTGTCTTA AACAAAAAAC 720 CCCAAAAACA AAACAAAAAG ACCCTATAAC GTTCTTTTTT TTTTTTCTTG AGACAGGGTC 780 TCTCTATGTC ACCCAGGCTG GAGTGTGGAG TGCAGTGGTG CGATCTTGGC TCACTGCAAC 840 CTCTGCCTTC CGCTCACCGC AACCTCTGCC TTCCAGGTTC AAGTGATTCT CCTGCCTCAG 900 CCTCCCGAGT AGCTGGGACT ACAGGCGCGC ACCACCATGC CCAGCTAATT TTTGTATTTT 960 TAGTAGAGAC GGGGTTTCAC CATGTTGGCC AGACTGGTCT CGAACTCCTG ACCTCAAGTG 1020 ATCCACCCAC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCCAC CATGCCTGCC 1080 CTCTGTGAGG TTCTTAAAAA GCCTGAAGAA GGGAGCTGGC AGACAGGGGA GAGGTTAGCA 1140 GTCTGCATAC TGGTGAGCAG GCCAAGGAAA GGACAAAGAT GGTCCTGGAG GGAGGAGGAT 1200 GAGGCCTTGG AGGAAGAGGA GGTGAGGAAG TAGAGTTAGG GAGGTGATGA TTTAGGAGTT 1260 GGGAGGGTCA TTCAGGAAGA GGAGTTAAGA ACCAGACAAG GGCTTTAAGA CCACAAAGAG 1320 ACATTCCAGG ACTGAGAAGG GGATTAGGGA TAGGAGACAG GTCTCCTTTG CAGCCGCAGG 1380 AGCCAGAGTA GGTCTCTGGA GAGACTCTGA TAGGGTAGAA GGGACACTGG GAGCTGAGTG 1440 GTAGTTACAG AGGGGCTTTT GGTATAGAAA GCAGTGTTTA AAGGACAAGA GGAAAGGTGC 1500 CAGGAATGAT GAATAACATC CAGGCCTGAT GTCCCTGTCT 1540
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