Tag | Content |
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EnhancerAtlas ID | HS121-31880 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr6:33768950-33771720 | SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Pou2f3 | MA0627.1 | chr6:33770465-33770481 | CTGTATGCAAATTCCC | + | 6.24 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GACAATGACA AGGAGCTCTT GTCACTAAGT TTGGGGTACA GTGGCAGACT GCTGTGTCCG 60 AGGCAGGGGC CCTCAGTTCT GGCCCATGCC CTACCTCTAG CTGTGTGATC TTCAGCCAAA 120 GCTCAGCCTG TCTGGATTTG GGCCTGGTAT CAGAGCTTGA GCAGATGAGC TCTGAGCACC 180 TTTCTGCCCC AGAGCTGTGG CAGCTGGCCA AGCTCCTGGG AAAGGCCATC CAGCTCCCTG 240 CCACACACCA GGGAGGAATC ATTTCACTTG TCCACCCTTC TCTTTTGTTA CAGGTAAGGT 300 CTTCTGGGGT CAGCTGGACT CATAAGGCAG GAGGGACCTC ATCTTTCAGA GAAGGAATGC 360 CTAGATTATC AACAGAACTG TGCCCCAAGA CCCAGAGAGA CCTCCCTGCC CCAGTGCCTA 420 TTAGAATGAC AAAAGGGGTG GACCCAAGCC CAGATGACCA GGGCTCTGCC TGGAAGTGCC 480 AGGCCAGGAC CCTGGGTCTG TAGAGCCTCT GCCATTGCAA AGGATGAGCC AGATGGAAAA 540 ATTCAGCATG GAGCTGTATC CCTGAGCCAA GAGGGCACCC CCTTCCCCGT TGGGGGAGCG 600 ATGGCTTGGG AACAAGCCCC CCGCCCCGTG CTCCAGTGCA TCTAGCTGCC TTTGGCCACC 660 ATCCTGAAAC AGCAGGGAGC AGGCTTCCTC TTTCCTCACA CCCTGGAACC CAGTGATTGC 720 TGACCAGGAA GCAGGTATGT GTGGAATGGC TGGTAGGACA TTGGGCTTTA GTGGGCTTTT 780 GGAGCTCGGG TCCTGGCAGG GAGCAGGTAG GCATGGTGAC TGCAGGGGTG CAGAGCCTTG 840 AGAAAGGGTC CACTGGGCAG ACTTTGGGCA GGGACAGGGT GGTCCTGGGG TGGGGGTGGG 900 ATGGCCTAGC TGAGTGCCAG CCAAGGTTGA CTCATTCAAA GGCAGCAGGG GCTGGAACCT 960 TGGCCTTTTG AGGCCCAGTG CTTTTCCCAA TACCCCACTC TACGTTGCCT CTGCCCATAG 1020 TAGGCAGAGG AAGGCACAGG GGGCAGGCCT GTTGAATGCA TCTTGGGCAC CACTGTTCCT 1080 GCGCTGGGTG GACTGCTGAG TGCAGGGGCC AGGCCTCCAA GCAGGGAGGG GAGGCCGGGA 1140 CAGCCCCTCC AGCAGTAGGG GTAGGGGTGG AGGTAGTTAC AAGGTTTCAG ATAAAGCGCT 1200 CCTCCAGTCC CCAGGCAGCC TGGATTCTGT CGGCAGGAGA GGGTCTGCCC TGGAAAGGCC 1260 TCGGGGCTTC TCTGCAGGTC TCAACCTGGC TCCCCCTTTG AACAGAACCT TCCAAGGCTG 1320 CAGGCTTGCA TCCTGCCTCT CAGCCAAGAC CTGTCTCCTC AGTCATCTGA AACCACCCTA 1380 CCACGCCAGA CGCTCCCTCT GCCTTCTTGC TATTCCAGCT CTCTCTTCTT CCCACTTCCT 1440 ATTTTCTCTC CATTTTGTTC AAACTCCATG AACAAGAACA ACAGAGCTCA GACAGCGAAA 1500 GCCTCCCCAT CCCAGCTGTA TGCAAATTCC CAGCAGGCTG AAAGGACCAC CCGCCCACCC 1560 AAGACCACCT CCCAGGAAGC CGAGGCCTTG TGTGCAGCCC CAGAGGAGCT TGAGCTGAAC 1620 GGAGAATGGG TTGAGGTGGG TGGGACCCAT CACTGTTCTT CCCTTCTCAT TCCTGCGCGT 1680 TCCCTGAAGA GTCTCTGGGG CCTGCTTTTC CCCCCAGCAG AGACGGATGT GTCACATTTA 1740 TGGCATCCCA TTTCCTTCAC AGAGAGGCTA TAGATCCTGT TTCATTCTGG TGTATTTAAT 1800 TCACTCCATA GGAATCAATA AAAACTTTAA ATTAAAAAAA AGGCAAAATC CAATTGCTTC 1860 TCATTTTCTT GATCCAACTG GCAGTCGGCA TGTCACCTAC GTTCATGTGT GTTCTGGTGA 1920 GCTGGAGGTG GGAGAAGGAG CTTTTCATTG TACAGTGAGG CACTAACTTT CCTTTCCCAT 1980 CATCAGAGAT GGGGGGCTTC AACCTTCAAG TGTCCAGCTC TGCATGAAGG GGGTGACCGT 2040 CTGCCCTCCC TTGCAGCACC CCTGGCCGGG CTAGCCTTGC CTCCCCATGT GCTCTCCCTC 2100 GGGGTCAACT TTTTCTTTTC CTTTTCTTTT CTTCTTTTTT TTTTTTTTTT CTGAGATGGA 2160 GTCTCGCTCT GTCTCCCAGG CTAGAGTGCA GTGGCGCGAT CTCGGCTCAC TGCAACCTCT 2220 GCCTCCCAGG TTCAAGCGAT TCTTCTGCCT CAGCTTCCTG AGTAGCTGGG ACTACAGGCA 2280 TGTGCCACCT CGCATGGCTA ATTTTTGTAT TTTTAGTAGA GACAGGGTGT CACCATATTG 2340 GCCTGGCTGG TCTCAAACTC CTGACCTTGT GATCCGCCCA CCTCAGTCTC CCAAAATGCT 2400 GGGATTACAG GCATGAGCCA CTGCAGGGCC AAATTTTTCT TACCTTTCCA GAGCAAAGCC 2460 ACCATGCCAA GAGGGGCCCT GCGCCCATGA TGAGCTCTGG CTTGGGTTCC CGGCCCACCG 2520 TGGATGTGCC AGACCCACCC ACAACAGCCT CTGCTTTGCC AGGAGTTGTA CCCACCTGCT 2580 TGCCTCCAGC GTCTGTGCCT CAGCCCTGCC TCTGCTCACT GATGCCCTGG GAATCAGCGC 2640 GGGCACTCAG TGCGAAGCCC GGCTGGGCAC TGGAAGGTGG CAGAGGGCCC TGGACCAGGC 2700 TGGCTCTGGC TTGCACCAGC GTTCTGCTTT AGGGCTTATG CTGACCACTC CCCACCCACT 2760 TTCTCCAAGG 2770
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