Tag | Content |
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EnhancerAtlas ID | HS121-11597 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr14:105354320-105355850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr14:105355196-105355206 | GGGGCGGGGC | - | 6.02 | NFIA | MA0670.1 | chr14:105354750-105354760 | GGTGCCAAGT | + | 6.02 | Tcf12 | MA0521.1 | chr14:105355683-105355694 | CAGCAGCTGTT | - | 6.32 |
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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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Enhancer Sequence | TGCCAGGGCG GGTGGGAGGC CAGGGCCAAG ACAGGGCTGC CAGTGGGTCT GCAGCATCTT 60 GGATGCCAGC TGAGTGCTGG CCGTGGGCCC CTGGTCCTGG CACGAGAGGA GCCTCTGTTC 120 CCAAAGCTGG GGTAGATGTG TTGCTGGACT CACGTGCACA CACACACGTG CATGGGCCGA 180 GGGCAGGGCC CGCAGTCCCC TGGTGTGGGT AGAACACCCT GACCATCTCT GGCGTGGAGA 240 GGGCCTTCCA TCCCCCAGGG TGTGCCTCAG GGCCCCGAAG CCCAGGCTGG CCCTCCCCAC 300 TCTTCCTGTA CTCCTGGCTC AGGCCCCTGG TGCCTTTGGG TCCCCACGCC ATCTGCCCAT 360 GGGCCTGAGG CCCTAGGCCT GGGGAGGGCT GTCCCATGGA TCTCTGCCGC AGTACTGTGG 420 CTCAGTGAAG GGTGCCAAGT ACACCTGTGC CCTCCGCTGG TAGCTGCTCT AACACCCTTC 480 TGAGCCCGCA GGCCCCATGA CCAGGGAGGG AGGGAGGGCT GTGAGCAGAG TCCTGCCCTG 540 CCCCCCAGAT GTCCATGGGC ACAGCAAGCG GGGATGGTCC TCTGTGGCCA CCAGAGCTGG 600 CCTCCTACCT GGGGTGGCCG GACATCCGCG TCTGCAGAGC GGGGCCCACC CCGCCCGCCG 660 AGGCAGCTGA GCTGTCCTGC GAGTGGATTG GTTTGAGGTC AAGGTGCTGC TGCTACTGCC 720 TTCTGCCCTG TGCACCCACC TACCCACCCA CGATCCCAGT GGAGCCTCTT TCCTGACTCC 780 CAGCATCCTC CCACAGCCCC ACCCCAACTG CTGGCTGCAC TGGGCAGGCC TTGCGTATGG 840 CTGGAGGCTG AGGCAGGGTT CGCTGGAGGA AGGGGTGGGG CGGGGCCGAG GGTCACCCCT 900 GCTTGGTGGA GCCTGCTGTC CCTACCCGAC GTGGTGCACT GGTGGTGTTT GACCCAAGCA 960 TGCGGCTCGC CATCATGCCC CGCTACAGTG CAGGAGCGCA GCTGCTGCCA GGCTTAGAGC 1020 AGGGGCTGGT GAGGAGGCCA GGACTCTGCC CAGGAGGGCG GAACCTGAAG CTTTGGGTCT 1080 GACAAACTCA AGCAGGCAGC AGGGAGGGAC TGCAGTGGCC TTGCTTGCGC TCTGACTGGT 1140 CCTTGCCTGT CTGTGTGGTC CAGCCTGGGC CGCAGCAGGT CCTGGTGGGG AGGTTTACTC 1200 TGTTTTGGGG TCTGTCAGGC ACTGCTTTCC CACCACCTGT AAGGGGGTTT CCCACCTAAT 1260 CAGCTGCAGA CTGCTCCCGG GTTGCAGCCA CTGGCCTGGG AGCACCAGGC CGCCTTCCCC 1320 GCATGTGCCC TGGGCTGGTG GGGGCCTTGT GGTCCCTGGA GCTCAGCAGC TGTTGATGTT 1380 TCAATGAAGG GCTACTGGGT GGGGGCACCA GCCTCGACGC TGCCCAGCCC TGCAGCACTG 1440 AGCCCTCTCC CAGAGGGACC CTGGGACTGC CACAGGGTGC TGAGTGCTGC TTTGTTCTGT 1500 TCTTGCTTCT AAAACCAATT CACTCACCAA 1530
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