Tag | Content |
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EnhancerAtlas ID | HS121-11069 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr14:68189430-68191180 |
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) |
EWSR1-FLI1 | MA0149.1 | chr14:68189545-68189563 | GAAAAGCAGGAAGGAAGG | + | 6.85 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH14I067721 | chr14 | 68188621 | 68189517 |
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Enhancer Sequence | TGTCTTAATT CAGCAACTCA AACAATCGTT TACAAAGACC TGCACTGGAA GCCGGTTCTC 60 AGCTGCTGAA AGAAGAGAAA GGGAAGGAGG CTGACAGAGG AGAAAGTCAG GGCAGGAAAA 120 GCAGGAAGGA AGGGGGTGTT GTGGATACCA TGGTGGAAAA CCAGAAGGAA GCATCTGCGG 180 CCGGGCAGAG GTGGGGCTGA GTTCTGGCCC CACCTGAGCT CTGGGGAGAG TTCTACTGCC 240 AGCGGAAGGC TGCATGGATG ACTCTGTCAA GTAGCTCAAC AAACACCTTA GGTGGGAGTC 300 CTTGCGTTTT CATTTTATTC CTTTGGGTGT CTCTGAAGAA CTCGGAGACT CTGTCCCTAT 360 TCAGGGTGGC CCTGCTGGCT TGTCATGCTG TTAAGTACCA GGTAGTTTGG GAAAGAAACA 420 AACTCTTCTG CCTTTGAGAC TACCCTCAAT TAATGTTTTG GGATGGCTTT TTTGCTGTGG 480 GATTTCTAGA GGTGTCAAAT AAAAGTGTGT TCTGAGTGGA GAATTTTTAA ATTTCTCTTT 540 TTTAATTTTT GCTCTGTCAC CCCAGGGTGG AGTGCATTGG TGTAGTCATA GGTCACTGCA 600 GCCTTGAACT CTTGGGCTCA AGCAACCCTC CTGCCTCAGC CTCCCAAGTA GTTGGGAATA 660 TAGGCAGGTG CCACTACACC CAGCTACTTT TTAAATTTTT TGTGGAGATG GGGGTCTCAC 720 TATGTTGCCC AGGCTGGTCT CAAACTCCTG GGCTTAAGCG ACCATCCCAC GTTGGCCTCC 780 CAAGATGTTG GGATTACAGG CATGAGCCAC TGGGCTCAGC CTAAAAAATT TCTTATGATA 840 AAGGAGGTTA AATGGACCTA CCAAGGACAG TGTTATTCTA GGTTCTCCAT AGAGATCTGG 900 GTTCAAGTCC CACTTCTGCC ACCACTATGT GACATGAACC TCCCTGAGCC TCAGTTTTCT 960 CTACTGTAAT GTGGAAATAA TACTGGAGAA GTTGAGAGGA TTAAAATAAA TTACATATGG 1020 AAAGTGCCTA GACTAGTAAT TGGCAGTCAG ATGATGTGCA GGAAATGTTA GTTCTGCCCC 1080 TCCGTATTCT GTTTTAGGAC CTGTGAAGTC AACTTCATGT AAAAGAGTGC TCTCTGCACA 1140 GAGGTCTGAA CAAAGGAGGT TTTCTCTCTG TTTGCCATCG GCCAGAATGA AATCTCTAAT 1200 ACAATGGCTG AAAGCCTCGG AAATGACCCA CTCCCTAAAA CTGGAGAGGC AGCCTAAGAT 1260 CAGTACCTGT GTATGCCATC CCCCAGAGTG CTAAGAGCAG TACCTGTGTG TGCCACCCCC 1320 CACAGAGTGC TGTTCATCAG TTACTCATGA TGATGGTTAC TGAATATTGA CTCCGCTAAT 1380 GTTTATCATG CATATGTTTT GAATGTAGGT TAGAGGGGAA AGCTTTCCTC TGGAACCTCT 1440 AGAGATAAGA GCTAGATGTA TTTATTATCT AACAAGGAAA GTCTCCATTG GCCCTGACTC 1500 CAGCATTTAC TCTGTTTGCT AATATGATTA TTTGTGGCTT CTGGGCAAGT GATCTTCCCA 1560 CCTGCACCGA TAAACAGGCG ACTACCTTGC CCCATGGAAA AATGTTGTCC TATGAAGGTT 1620 AGCTTTTATG AGTCTCCTGA CTGCAACTTA AAGATACCCT TCTTTGAGGC TGGATAGAGT 1680 TTTTTTTTTT TTTTTTAACG TATCTTAGTG TGAGCTCGTG AAGGATGGTA CGTGATGCTC 1740 TTGTTTCCCT 1750
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