Tag | Content |
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EnhancerAtlas ID | HS121-17883 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr18:21512260-21513740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr18:21512560-21512571 | GATTGTGCAAT | - | 6.32 | ZNF263 | MA0528.1 | chr18:21512951-21512972 | GGAGGTGGGAGGGATGGGGAA | + | 6.34 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGATCCTCTC TTTGTGGGTA ACTGATGAGA ACGGCCTGCC CATGGGAAGG GTATCTCTTT 60 GGTCCAGTTA ACAAAGTCAG CTTTGTCAAC ATGTGCTGCA CGAGACCCGC ATACCACAGT 120 CTTTCAAAAT GCCATCTTTG GCAAGATACA CCCATTAAAA AACCCATAAA AAACTCCTGG 180 GCCCGGCCTC CTTTTGGAGG AGCAGCGTTA GCATGTAACC TTGGAAAAGA CCTAATTAAA 240 ATTAACTTCA GATTATGGCC CGGAAAAGTA TTCACTGGAA TTTTATTGCA TTATAATCAA 300 GATTGTGCAA TTAGATTTAA TCAGCTCTCC ACGGTTTTCA AGGCCAAGGA ACTGCATGGA 360 CCAGTGCTGT GCTAGGAAAC CAAATCACCA CAATGTTGAA CGTGATATTT AATAGAGAGA 420 GAGTAGCTCT TGGGGCTTCC ATGCAAGTGT TTACATATTT TTTTTGATAC AAAATTATTG 480 TTTTTAGATA AGAGGCAAAA TCTTCTCCAG GGTAAGGAGA GGGCCTGGTT CTGGCTATGA 540 ATCTCAGGCT GGAATTCTCA GGCTACCATG ACAGGGAGCC TCCCACCCAT CAGGGCTCCA 600 TCCTCCTTGG CCAGGATGAG GCTTAGAGTT CTCATTTCCC TCCTGGTTGA TGAAACATCT 660 TCCTTGAACA TCTAATTCAG GGATTGGAGC AGGAGGTGGG AGGGATGGGG AAGGCCCAGG 720 GGTTGTTAGC AACAGCTTAC TGCCATGATA AGGCTTGGAC AAGAATCGTG AGATAAAGCA 780 AATTTGTCCA AGACTTTCCT CCTCATAGTC AGATAAATCC TTCCATAAAC TCACCTCTGA 840 AGTTTCCTTA TATTTACCAT CATTCAGTAT CATCCAGTGC CCATCTTCTC CCTCTGTGCA 900 TATTTTACGT TCGTATTTCC ACATGACACC CATTTCAAAG AAAGAACTAT AGTATCCCGG 960 CCCTCCCACA ATTCTGCCAC AATCCCAAGT CAATAAAGGT TTCTTGGGCT CCTCGCCGGC 1020 TTCTAGAGGT GATATTAAAG TAGGAGATGA AAGTTTCCCT AGGAACCATG ACCATAAGAA 1080 TGTGTAATTT TTAAAAAAAT CATGGATACA TAACAGTTGT ATTAATACAC ATTTATGGGT 1140 TACATGTGAT ATTTTGATAC AGTTCTACAA TGTGTAATGA TCAAATCTGG GTAACTGGAA 1200 TGTGCTTCAT TTCAAGCATT CATCATTTCT TTGTGTTGGG AACATTCCAA ATCTTCTCCT 1260 CTAGCTATTT TAAATTATAC AATAAATCAT CATTAACTTG AGTCACCCTA TTGTGCTGCC 1320 AAACACTAGA TCATATTCCT TCTATCTAAC TGCATTTTTG TACCCATTAA CCAACCCCTC 1380 TTCATCCCCA AAACATGTAC TTTTTGAAAT GAGCTCTCTC TACCAGAGGG TCTTCCTCGA 1440 CATGTCCAAG TTTGGCAGCA TCTTTCATTT CTGCTCTTTT 1480
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