Tag | Content |
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EnhancerAtlas ID | HS121-19956 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr19:19014230-19015570 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr19:19015236-19015257 | ACCAGGACCCTGGAGAGCAAA | + | 6.41 | Zfx | MA0146.2 | chr19:19015017-19015031 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCCTGCAGGG AGGGTCCCGC ATCATTGCCT GTGCCCCTGC TGCCCGGCCC TTCCCCCGCC 60 AGCCCCCTCC CCTAGCGGGG GGGACTCCAG CACTGCACAG AGACGAATCT GGTGTGCCCG 120 GTTCAAGGCA CAGCCACTCC GCCATGGGGA CTACCCGTAA CTTGTACTCT GCTGATGGGG 180 CCTAAAGACT CGTGGCCGCC TCCTGCCCCA CCTCCCACCC AGCTCCCGGA GTGCTGAGTA 240 CACAGAGGTG GAATCTGGGG CTTCCAAGGC CTCAGTGCAC AGGTGGCTGG CTCAGGGTCT 300 GAGTGGGGAC CACTGGGTCA CTGAGCACGT CAGAGGAGGA GGAGTCAGCT CTGTGACCAG 360 CAGCCCTGAC CTGTCCACTT GCTCAGAACA GCAGAACACT TGCAGGGGGA GCCTGAGGCC 420 AAGGCAGGCA GTGAAAACAG CCCAAACTAC CCGATAGGTC TGCCGGGGCC TGTCCTACCA 480 TACTAGACGG TCACTGGAAG TCTGTCTGGG TGAGGCTTCA GCCCCGTGGC GGGCAGGGAC 540 GGGGAGCACA TTTTTTTTTC TTTCTCAGAG TTTCACTCTT GTTGCTCAGG CAGGAGTGCA 600 CTGGCGCGAT CTTGGCTCAC CGCAACCTCC ACCTCCCGGG TTCAAGCGAT TCTCCTGCCT 660 CAGCCTCCTG AGTAGCTGGG TTTACAGGTG CATGGCACCA AGCCCAGCTA ATTTTGTATT 720 TTTGGTAAAG ATGGGGTTTC TCCATGTTGG TCAGGCTGGT CTAGAACTCC CAACCTCACA 780 TGATCCACCC GCCTCGGCCT CCCGAAGTGC TGGGATTACA GGCGTGAGCC ACTGCGACCA 840 GCCAGGAAGC ACATTTTAAT AGGCCCACAC AAAAGAGTGG CTCAGAAGGG GGCCAAGTCC 900 CAGAAACCAG GAGAGGGGCT GTTGCCGGGC GGAGGTGCCC AGGCCTGGGA GCTGAGGACA 960 TCTCCACCGC TGCTATGGGA ACACTGAACT CCGTCCCTGG CTGGCGACCA GGACCCTGGA 1020 GAGCAAAGCT GAGTCGCAGA AAACCCCAGG AAGCCCTGAG GGGAGGAGGG CCTGCCAGGC 1080 CAACCCAGAC CCTCGAGTAC CCCTGTGCCT CAGGCTCAGG AACCCGTCCC CGCCCCCACC 1140 ATCTCTTCGC TCTGGCTCTG GCCAAGTCGC TTGGCTGTGA GAAGCCCGGA ATGGAGTCAA 1200 GGCTGAGTTA TGCCAGGCTG GCAGGGGCCA CGGCCTGATC CTGGAGCCCC ACTGGAGTGG 1260 CCAGCAGCCT ACGCACAGGT GGGGGTGCCC ACAGACCCTG CTCAGCCAGG TGCCCGCAAT 1320 GCCCACCCAC CTCATGGCCT 1340
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