Tag | Content |
---|
EnhancerAtlas ID | HS121-05658 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr10:134008510-134010360 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr10:134009704-134009718 | CAGGCCCAGGCCGG | - | 6.71 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGGTGAGGG TGGCTGGAGG GGCTGGAGGG CGGGCATGGA GCCTGGTGGA GGAGCCTCTG 60 CCCTGACCCT GTGTTCTGCC GATGGTGCTG CTCTGCCCTG GGGGCTGGTG TCCAGGTTTG 120 AGTGGAAGTT GGAGAAAAGT CATTTGAAGG CCCATCCCAC CTTCAAAGGC TCTAGACCAA 180 GAGGCCTTCT CTTTCCCAAT CCGAGGGACC CATCCTGGAA TTGTCCTCCT GATGAAAAGA 240 TGCAGCAGAT CCGTCGTTTC TTAGAAGAGA GGCTGCCCAG GGTGGAAGAG CAGCAGTTCC 300 CCAGTCTCCT AGCATCTGGG GATCCTTTCA GAGGGAGACC CTTTTAAATC CATATCTCTT 360 TGTTGTCACC AATGCTAAAA CAGATCAGTC TATAAACAAG TTAACATTTT TCCCCACAAA 420 AAACCCTGAA GCTAAAACTA CATCAGAGTT TCATAGTGGG TTTGACAAGT GGCATATCTG 480 ATTATAGCCG ATCTCTCCTA ATCTGAGTCC GGCCCACAGC TTCCAGCCTG GAGGTGGGGG 540 CGGGATGGGG TCCAAGCAAG CCCAGGAGCC TGTCAAGGCC CTGGCACTCC CAGGGATGCC 600 TGCTACCCGT CCCCTACAGA CCTGAAGGAG GCAGGGGCAT TTCTTCAAGG CCATTCCTCT 660 GGGTTCCCAT TCCTCAGAGG GTGACGGTCA TCACATAGGT GCCCCTTGAT GTCAGGACCC 720 CTCACCTCCC TGCCCGGGGG CTGGTGGAGC CCGTCAATCC TCAGTCCCTG GGCCTCACTC 780 CAGGCAGCTG CTCTGCCACC CATGCTGTTC TGTGAGTGGA CTCGGGAGGC CTGTGGCCTC 840 GTGTCTCAGA GCGGAGGTGG AAGCAGGGCC TGCACCTCCC CTCACCCTGT GTTGGCAGTG 900 CTGGGGCCTC TGCTCCCCAA GAGCCATGCA GGAGTCCTCA GTCCTGTGCC CACGGGGTAG 960 TGTTGCAGGG ACAGCACTGC GCAACCCAAA CATGACCTTC CTCAGACACT CGGGGGCAGG 1020 CCTCAAACTC CAGGTCACAT ACAGGTTGCT ACCTGGAGGG ATGGCTTGTG GGGCACAGTG 1080 TGACTCAGTT TCCCCAGTGT GCCTTAGCTT GTCACACTAG CACTTTCCAC CCAGCGAGGA 1140 GGAGATGCCA TGGGTTGGGT GGGCTTGAGT GATGGGAGGT TGGGATCCTG CCTCCAGGCC 1200 CAGGCCGGTC CCCACACAAG TTCCGAGTCC TGGGGGAGGT GGATGGGCTG TGGCTGCCCA 1260 GGAAACAGGA GAGCTCAGCC CTCTTCCTGT TTGGGCCCCA ACGTCAGAGG CAGCCCCTCA 1320 TCCTTCTGCT CGTCCTAAGG GCCCAGCCCT GAGATCTGGG TGGTCCCACA AGCCTGCACT 1380 GTGAGCCAGG CATGGCAAGT GGGGCTCCAA GGCCCTGCAG GCAGGTGCTG GATGTGCTGG 1440 ACGGCCAGAA TGCAGGTCCC CAGCACAGCG CGGCCCTGGC CGCACTTCCA GGAGGGAGCC 1500 AGTGGAACCC AGGCCGAGAG CCCAGGCACA GCGGCTCTTC CAGTAACGGG GGGTCTGCTG 1560 GATGGGTGTG AGGGGTTCTC ACCTGCATTT GCCGCTGGGT GGACAATCAG TTCCTAACCC 1620 GGAGCACAGG AGCAGGCAAG GAGGGCCTGG ATGTAGCTGC CTCCGCCTCA CTTCCCAGCT 1680 TGCTGGTGTG TGCATGGAAG CGGGGGACTG CTCCCAGGGC TGGCAAGCCA GTGAGGGAAG 1740 CACTGCGGGG GAGGGGCCCA AGACCCCCAA CCCTCCAGTG GGCAGGAGCA GCAGAGGCTC 1800 CGTAGGTTGT CTGACTGGTG ATGGCTGAGC CTCTGACCCC TGCCTCTTCT 1850
|
| |
|
|
|