Tag | Content |
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EnhancerAtlas ID | HS120-02794 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr17:44050340-44051750 |
Target genes | |
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) |
ZNF263 | MA0528.1 | chr17:44050372-44050393 | CCCTCTATCTTTCCATCCTCC | - | 6.33 | ZNF263 | MA0528.1 | chr17:44051642-44051663 | TCCCCTCCTCACTCCTCCTCC | - | 8.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_06294 | chr17:44050389-44056465 | Brain_Hippocampus_Middle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 44050369 | 44050419 | chr17 | 44051294 | 44051433 |
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Enhancer Sequence | TGGCTTTTGA GTCACTAGTT GGCAGTATCT GCCCCTCTAT CTTTCCATCC TCCCCATGGA 60 GTTTCAAGGT TCCTTTCTCA GTACTTCTTC AGGCTCTGCA CGTTCATTTG GATCTTGTGT 120 CTTGGGGTGA AAAACTGGCC CAAGTGTCTC CCCAAGCATC CACCTTTGGA TTAATTTGGA 180 AAATGGCTGT CAAGTGCCCG CCTCTTGCTT GGTATAATGC TACAGCTTTA GAGGACGCAG 240 CAGGCATGGG CCTTGCCGCT GAGGTTCTTA GCCTCATGAG AATATCCAGA TCAGATTCTC 300 TTGGCTCCTT CTTAGAGCCA GTGATGCAAG ACACTTCCTG CTCATCTTGT CGGGACGGTT 360 TTACAAGTTG CCTGCCATCC TGAGAAAGTC TACAAAACGA TGCCAGACCT CATGCCAGCT 420 TCCCAAGCCT TGACTCTCAG TGCTCCCTCA ACAGGATTCT GGAAGAATCT CCCAAACAAG 480 TCGCAATGCC CTCTGGACCC TGTGCAGGCA TGAGACTCAA GAGCATTGGC TCCCACCCCT 540 GGTGGAGGGA ACACTGCTGG GGCTGGGATC TTGCCTGGTT GCTCCGCCTG CACCCAAGAC 600 AACCATAATT AAAATGTCCT TCATTGAACT TGGAAAGCCT TCAAAGCTGA CAACTCCTTA 660 TGTGTACCCG GAAAGGCCTG GGAGTGTGCC AGGGCATTGC TCGGGAGGGA CGCTGATTTG 720 GAAGCATTTA CCTGATGAGA GACTGACAGC AGCTCCTGGT AGCCGAGCTT TCCCTCCTGC 780 CTCTGCTGTG AAGGTGGACC CATCCAACAG TCAAATGCCT GACTCTGGAC AGGAGCGGAC 840 CTATTTATTG CCATGCAAGG GACTCTGCAC TTTTGAATTG TGGGTCATGG GCTTGGATTT 900 AGGGGTTAGA GCTGGGAGAA GTCTTGGAAG TCACCTAGAG ATGACACTGC CATTTTGCAG 960 ATGAGGAAAC CGTCCAATCA AAATGGACCA AGGACTTGCC CAAAGCCTCA CAGCAAAACC 1020 ATAGGCCCCC GCACTAACCC CAGAGTCCCT GTGCTGTCTT AAGGATCATA TAGTTGTAAG 1080 CAATCATCTG GTTTTCAGTA TTTCTTCTTT TAAAATGCCT GGGGCCATGC CCAGCAGTCT 1140 GTTTCACTGC AGCGTTTACA CAGGGCTGCC GGGCTTTCCT GGTGGATGAG CTGGGCGGTT 1200 CATGAGCCAG AACCACTCAG CAGCATGTCA GTGTGCTTCC TGGGGAGCTG GTAGCAGGGG 1260 CTCCGGGCCC TACTTCAGGG CTGCTTTCTG GCATATGGCT GATCCCCTCC TCACTCCTCC 1320 TCCCTGCATT GCTCCTGCGC AAGAAGCAAA GGTGAGGGGC TGGGTATGGC TCGTCCTGGC 1380 CCCTCTAAGG TGGATCTCGG TGGTTTCTAG 1410
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