Tag | Content |
---|
EnhancerAtlas ID | HS121-18988 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr19:5668490-5670770 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:5668812-5668827 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr19:5669889-5669910 | GGAGAAGGAAGGGCAGGAACG | + | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 5669960 | 5670070 | chr19 | 5669230 | 5669376 |
| Enhancer Sequence | TTAAAGTGTC ATTTCTTTAT TTCTGCCTCT TTAAATGAAA CGAAATTAGA CTTTTAGTTG 60 TATTGATATA CACTGATTGT TCCTTTTTTT AATTATTATT ATTATTTTTT TTTTTTTTTG 120 AGATGGAGTC TCGCTCCGCC ACCCAGGCCT GAGAGTGCAG TGGCGCGATC TTGGCTCACT 180 GCAGCCTCCA CCTCCAGGGT TCAAGTGATT CTTCTGCCTC AGCCTCCCGA GTAGCTGGGA 240 CTACAGGCGC CTGCCACCAC ACCCGGCTAA TTTTTATATT TTTAGTAGAG ACGGGGTTTC 300 GCCATATTCG TCAGGCTGGT CTTGAACTCC TGACCTCATG ATCTGCCCGC CTTGGCCTCC 360 CAAAGTGGTA GGATTACAGG CGTGAACCAC CACGCCAGGC CGACTCTGTT TATTTTTAAA 420 TATGTGTGAA ACCTCTGGGA AGGCATCCGG GTGTGGAAGA GGCTTTCCAG TGAGACAGTG 480 ATTGGTTTTC GCATAATGGG CCTGTGCGGT GCAGGTTTTG CCTGACTTCT CAAGTCACCG 540 AGTTCTCCTT TAATGTTAGC ACAGACCGGG CTGCTTTGCT CTTGGGTACT GGGTGGCATC 600 CCTGTCAGGG TGTGGGGGTC TCAAACCCTG TTGATGGACA CTGGCGGATG CTTCCCCTGC 660 GGATCACACT CGAACCAAGC CTGCGAAGAT TTCCAGCTGC CACTCTCCAC ACTGACTTGC 720 CAAAGCCCAG GCACCATCAT CATGTGGATG CTTCCGCATT ACCTTTTTAC TCAGAGGACA 780 AACTATTTTC ACGGCAGAGT CGGGTGGAAG CAGTGAAGGC TGAAGGTCAT CAGCAGCATC 840 TCAGGCCCGA GGCGTGCTTG TGCACAGGCT CAGCCCCCTC GTGCCAGGAT GGGGCTCTGA 900 CCAGCCCAGG GCTGGCCTCT GTGTCAGCCG GAAGGGACGA GCCCAACGCC AACCCTCCAC 960 ACACCAGCAG CAAGCTGGAG CCACGGCATC TGGGATCCAG CACCTGTCCT AATCCAGGAA 1020 GCCAGGCCAG ACTTGGGACA TACCTCAAAC TGTGAAGCAA GTGCCTCCCC CATTTTGTAA 1080 GCCTCACTGT AGTGGAGAGC GGGGAGGAAG CAGTGTCCAG CAGAGAGGAA GACGGCGGAG 1140 CCCCAGTAAC GCTCTAGGGT CCCTTCAGCT GCAAAGGACA GATGACCCCA CCAATACCAG 1200 TGGTGGCTTA GATGGTAAAG GGGGGCCCTT TCCTGCCTTA ACGGGAAGTT TGTAGGTAGG 1260 CAGTTCCCGG GGCTCACTGC AGCCCACCTC AGGCTCTGTT TCTCTGAGGA TTTTGGGACT 1320 CTCATGGATG ATGGATGGCT GAAACAGCTC CAAAAATCCT ATCCACCCAC AGTGTGGGCA 1380 TCATCGGGGC TATCCAGCAG GAGAAGGAAG GGCAGGAACG GGGACTTGAA CTCACAGGCC 1440 TCTTGGCAAA CTTACCCCTG AGGCTCCTTA GCCAGAACTC GGTCCTGTGC TCGCCTTTCT 1500 TGCAACCCGT CCCTGGCGAA GACGGAATGT TTCTCTTCAG AAGGGATGTG ACATCCGGGA 1560 AGGAACCCAG TGGTAACCCC CAGCAACCAC GTTCTCAGCC TTCCCCTCGT ACCTTTTTTT 1620 TTTTTTTTAA ATTCAAGCTG TTCACATTCT CTGTACTTTT TTTTTTTTTT TGAGACAGAG 1680 TCTCCCTCTG TCTCCCAGGC TGGAGAGTGC AGTGGTGCGA TCTCAGCTCA CTGCAGCCTC 1740 TCTCTCCTGG GTTCAAACAA TTCTGCTACC TCAGCCTCCT GAGTAGCTGG GACTACAGGC 1800 GCCCACCACC ATGCCCAGCT AATTTTTGCA TTTTTAGTAG AGACGGGTTT TCACCACATT 1860 GGGCAGGCTG GTCTCAAGCT CCTGACCTCA GGTGATCTGC CTGCCTTGAC CTCCCAAAGT 1920 GCTGGGATTA CAGGTGTGAG CCACTGCACT CGGCCCCATT TTTTTTTTGA GCCATATGCA 1980 GTTGTGCATG CCAGTAATCA ATCCCAGCTA CTTGGGAGGC CAAGGCAGAA AGATTGCTTA 2040 AGGCCAGGAG TTAAAGTCCA GCCTGGACAG TATACCAAGA CCCCATTTCT TTGGGTTTTA 2100 GGGGGTATTT TTTGAAATAA GAAATGACGG GCTGGGTGCG GTGGCTCCGG CCTGTAATCC 2160 CAGCACTTTG GGAGGCCAAG GTGGGTGGAT CACCTGAGGT CAGGATTTTG AGACCAGTCT 2220 GGCCAACATG GTGAAACACT GGCTCTACTA AAAATACAAA AATTAGCTGG GTGTGGTGGT 2280
|
| |
|
|
|