Tag | Content |
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EnhancerAtlas ID | HS195-07442 | Organism | Homo sapiens | Tissue/cell | VCaP | Coordinate | chr9:138874730-138876180 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr9:138875970-138875991 | GGAGGACAGGGGAGGGGAAGG | + | 6.53 | ZNF263 | MA0528.1 | chr9:138875967-138875988 | AGAGGAGGACAGGGGAGGGGA | + | 7.05 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr9 | 138875644 | 138875800 | chr9 | 138875800 | 138876074 | chr9 | 138875907 | 138876133 |
| Enhancer Sequence | CAGAACCCCA CTGATGGCCG CAGCCTGCCC CCTCACCCAC CTGTCCCCCA TCTCGGTGAG 60 GATAGCAGGC ATGTTCTGCC ACCTTGTTCC TGCCTCCGTC CCGGCTGACC CTGCCCCCTG 120 CTGTAGGCTG GCCCAACGTC ACACCTGGTA GCCTCTTGCT GCTCCGTGGC CTCTGAGGCC 180 CCAGGCACAC GCTGGGTCCT GTCCAGCCCT CCCCTCTCCT GCACTCCAAG GGACCCCTCC 240 AGGGGACCCC TCCTTGCCCA GCAGCCGAGG GGGCTGCGTT TCCCAGCTTG TGCCCAAGAG 300 TGGCGCCCGC GTAGTAATTC CTAATTAAAT AGAGCACAAA ACAGGGGATT GTCTAGCGAT 360 TAGCCAAACC GACTGGATTT TGAAGAACAA ATATCCCGTT AGCACTACTT CTGCCGAGTC 420 CACATGGCCA TGAAGCAGAG ACATACGGGA GCTCGGTAAT GAATATGGAA ACCTTCTTTT 480 CTGGTGTTGC TCACTCATAA ATGAAGCTGC TTTATGGAGC ACGAGCAGAG GGAAAATGAC 540 TGCGCCCAGC CTGATTTATC TGCTCAGACG CTTTGTAGTG CTTCAGATTA ATAAAAATAT 600 TTAATAAAGA ATCAAGATGG TTTATCTGTA ATGCAAAGAG AATCACATTG CCTATATTTT 660 TATTACAGAA AAATTGGAAG CAGGAAGAAA TAATGATATA AGCTACTGTA TAAATGACAA 720 AAATACCCAT TCTGGTTATG TGCTTTGCGC TACAATCCCG CGCCGCCCTA TAAACATAAT 780 CTATTCGCGT GCCTCTTTCA GCTGATTCCA GAGCCTGCTC TGCACTGTGG AGTTTAATAT 840 CACCCTGTTC TCAACTGCAC AGGGAAGTGA TTAAATAAGA AATAAATTCG GCTGTCATTG 900 CATTTAAAAT CAAATCAAGG ATCATTTGTT ACTCCAAATG AAGCAGTTCT CCTTCCCTGC 960 CCGTAAGTAG GCTGCTGTTC GCTGAACCAT TTAGGAATGT ATATATAGTA AACTCGCCGC 1020 ATAATGCCTT GTACTCTGAT ATGATCTTTA TGGGGCCGCT CCGAGCGCGG GGAGCGCCCA 1080 TAAGCAGCAC ATGGCTTTTT TAATTTGAAG TTACAGGTAT GAGACTTCGC AGTCCATCCA 1140 AGTCTTATTG GAGGGGACCC ATGTGAGATG TGGGGGCCAC TGCCCAGGAC CCCTCCCCCT 1200 GCACCCCTGC TCAGCTACAA CCAGCCCTCC TGTCCTCAGA GGAGGACAGG GGAGGGGAAG 1260 GAGCTAAGTC AGGTCCTCAG CGATGCACCC CTAACCCCAA CCCTACCCTA AAGGGCAGGA 1320 GGGGCTGGGA AGCCGCTAAG AGGCGGGAAC TGGAGGAGAG GGCTCTGCTG GGCTCCGTAG 1380 TGGGTGGGGA GTGCCGGGCG ATGGGATGGC ACAACGGGCC CCATCCTGTG CATCCTCCTC 1440 ACCTAGAGTT 1450
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