Tag | Content |
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EnhancerAtlas ID | HS121-24406 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr20:62224440-62226960 |
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) |
ZBTB18 | MA0698.1 | chr20:62225473-62225486 | ACACATCTGGAAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 62224745 | 62224846 | chr20 | 62225035 | 62225115 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I063593 | chr20 | 62225222 | 62226088 |
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Enhancer Sequence | GCCGAAAGGG AACCTCGGGT GAGTGCTGTT TGGACCACAG TCCCACACCC CACATACCCT 60 GTCCACCCTC CTCACACCAC CTTCTGAACC TTTCCATCTG TCTTCACAAA ACTGACAAAC 120 ACAGGATACG CACTAGTACA GCCAAAGTGT ACCTGCCTTA TATTTTATGG CTATTTTTAA 180 TCACAGACGT TGTCAAACAT ACAAAGGAGA AACAACGCAG AAACAAATCC CTTGAACCCG 240 TCACCCAATT TCAGCAAATC CTCAACACTT TCCTCCTCTT GTCCATTTAC GATTGTACTC 300 AACAAGCACT TTCGACTGGA CCGTCAGGAG CGAGACAAGG TGATCCTTCT GCTTGACTTG 360 TTTTCCCACC GAGAGCTCTG CGGCTGCGTC TGTCGCCCGT GGGGCTCGCC CTCACCTCGC 420 CTCTTCAAGT GATGCTTCAT TGAAGTCATC ATAAATCTCA GTATCTATCA TGTTTCCATT 480 TTTCTACACC AGAACAAGTG GGGCTTTGAG AGACAGAAAC CGTCCTGGCT CTTCCTGTGG 540 GTCCCTCTCT CGCGCCTGCA GAACACAACT GGGCGTGTCG TTCATATGTG GCCATTTTGG 600 GCGTTGCTGA TAGAGACTTT ATACACAGAT CTGGCTTAAA AAACAAACCC GGGGCCGGAT 660 GTGGTGGCTC ACGCCTGTAA TCCAGGCACT TTGGGAGACT GAGGCGGGTG GATCACCTAA 720 GGTCAGGAGT TCGAGAACAG CCTGGGCAAC ACGGCAAAAC CCCGTCTCTA CTAAAATACA 780 AAGTCAACCG GGTGTGGCGG CGTGCGCCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG 840 GAGAATCGCT AGAACCCGGA AGGCAGAGGT TGCAGTGAGC CGAGATCAGG CCCCTGCACT 900 CCAGCCTGGG CGACAGAGCA GGACTCCTTC TCCAACACCA CCACCAACGA CCTGGAAGCA 960 GTTGAATGTT TTGGGAATAC TGGCCTTTTC CACATTCATC AAAGACATGG CAGTGGTGAG 1020 TATGACTCAT ATTACACATC TGGAATTATT TGGGGCGTGA ATGAGTCGTT TTTCCGAGTT 1080 GGGGCTGGCA CAGCATCTTT TACTAACTGC ACAGTAGCCA AGTCAATGGT TCTCAGAGAT 1140 TGCAGGTTAA AGAACCCAAA TCATCTTCAG AAGAGCTGAG CCTCAGCCTA GCTGTGAGGC 1200 ACTGACTACA GGGCGTGGAA GGCCCAGTTC CTTCCCTGGC AGGCGGTCAG GCAGGGCCAA 1260 CACTAACGCG GTGGAGCCGC TGGGGAGGCC CTGGGGAGGA CAGACAGGAG GCTGGGCTCT 1320 ACCCAGCCCC TCTGACCACA GCAGCCCAAG TGTCCTGGGC TTCTCAGGAC TCAGCACTGA 1380 ACCTGCCAGG CTGCCCCAGC AGGACGTGGA AGGGGGCCCA GGAGAAGGGT GAGGCCTCCC 1440 TAGTGCCCTG GCCTCACTCT CCTACCCAGC GGGACAGGAC AGGACTCAAC TGGGTCCCAC 1500 CTGGGCCAAC AACAAGGACG TCCCTGGGCA CACAGGAACA CAATCTGGCC AGCAATGCGG 1560 AGTGGCAGCT TAGGGACAAT GCATGTGGCA TTGCTGGAAA CACATCACCA AAGACCACCC 1620 AGAGATGTGA CCAGGGAGCC CAGGACCTAA CTTCACTTTA ACTTCAGTTT TTTTGTTTTG 1680 AGATGGAATC TCACACTGTC GCCCAGGCTG GAGGGCAGTG GAGCGATCTC AGCTCACTGC 1740 AACCTCCGCC TCCTGGGTTC AAGCGATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGGACT 1800 ACAGGCATGC ACCACCACAC CCGGCTAACT TCTGTACTTT TAATAGAGAC AGGGTTTCAT 1860 CCTGTTGGCC AGGCTGGCCT CAAGTGATCC ACCCGCCTCG GCTTCCCAAA GTGCTGGGGT 1920 TACAGGTGTG AGCCACCACA CCCAGCCTAA CTGTAGTTTT AAGAAAAATT TCTCTATTCA 1980 TAAAGCTGGA AAGAATTCTA GGGAACAACC TCTCCACAGT TTAGAGCTAC AGACACCAAC 2040 GTGGAACAGT ATCTAAAGCG TCACCCAAAA ACCCAAGTGG CAGGAATACC TGCAGCAAGG 2100 CACCCAGCAC GGAAGGCGGG AGCACAGGCG CGCAGTTCCG TAAACCGCCA GGTCAGGAGG 2160 GAAGCGGGTC CAGATTTGGG GCTGGGCCGT GGGGGTGGGA GGGAGGGGGC CGGGTGGGCG 2220 CCCAGGCACT CTCTGTTACT CGCTATACCC TTCCCCACAC GTGAGTTATT ATATTACAAC 2280 CAAAATGGCT TAAAAAGAAA AGTGCTTCAA TCTTCCTTGT CAATGAAAGC AGCAATTCTG 2340 CCAGATCTCC TCTGTGAGGC AGGAGGAGGC TGATCCCAGA CAACTCAGGG TCCCAGGCAG 2400 GAGACCGGCA GTCCTGGCGT GAGCAAACGC CTGGGGCCAA GGAGGCCACC CAGGGGCATG 2460 TCACCCTCTG TGGCCATGGC CAGGGTGGGG CTGGGTCAGG ACGAGCAGCC CTGTGCACCT 2520
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