Tag | Content |
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EnhancerAtlas ID | HS121-36252 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr8:144697090-144698270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr8:144697813-144697827 | CACCACGCCCCCTT | + | 6.39 | KLF16 | MA0741.1 | chr8:144697814-144697825 | ACCACGCCCCC | + | 6.14 | SP1 | MA0079.4 | chr8:144697811-144697826 | TACACCACGCCCCCT | + | 6.07 | SP3 | MA0746.2 | chr8:144697813-144697826 | CACCACGCCCCCT | + | 6.29 | SP4 | MA0685.1 | chr8:144697811-144697828 | TACACCACGCCCCCTTC | + | 6.39 | SP8 | MA0747.1 | chr8:144697814-144697826 | ACCACGCCCCCT | + | 6.52 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGTGAGGC GGGGACAGTT CAGGCTCCCC AGGCCAGATC CCAGCCCTTA CCTGCTCCTC 60 CAGACGCAGA AGTGGAGACA CACCCTGGCC CTTCAGCCCT GGGAGGACCC AAGCCTGCCC 120 ATCCTAACCG TTTCCGGACA AGGCAGTGGG CTTACAGACA CCATTGCTCT CCAGCCCCAC 180 CAAGGCTGGA GGAGGGGCTG GCTCTGCCTT CCACTATGAG GAGAACCACA CCCCCAGCTC 240 AGGGCTGGGC CCCACCCAGG AGGCTGCTGA GGTCAGGGCA TAGGACCCCA CTGGAGGCTG 300 GGAAGGAGCC CAGTCTGGCC CTGGGCTGGG CTGGGGCTCC CACTACACGG GGAACAGGGC 360 GGTCTACTTC CCCACCCTGG AGGAGCTCCC ACCTGGCTCT ACTTCCCAGG ATCAATGGAG 420 CCTGCGCTTG CCGGGTCCAC CCCGCGGGCC CCACTTCCCG TGCATGAACT AGACACGGCA 480 TGGCTGGAGC CCTGGGACTG GTCTTGGGAG AAGGGAGAGG TGGTGGCCAG GCAGCCTGCT 540 GGGAAGGCCG AGACACCGAC AAAGAGGGCT CTGGGGTGAC AGGGCTCCTG GGCAGAATCT 600 CCTCTGAGCC TCTGCTCACG CTAGTGCCTC CTACGCTTAG CAAAGCCAGC TAAGGCAAGG 660 CTGCTGCCCA GTGACTGGTG GGGCCAACCC TCCGGAACAC AGCTAGCCAC GGCAGGGCCC 720 TTACACCACG CCCCCTTCCC CCAGACACAG GCAGCAGATG CACAGAGCGC GGTTCACACC 780 CCTGCACCCC AGAGTGTGTG GTGGGCCCGG CTAAGGGGAG CTGGGCCAGC ACAGTCCTGG 840 GAGCCAGAGG CTCCAGAGGC CCTGGGGACT CAGGGGGCAG GAACCAGCTC CCAGTCCCAC 900 GTGGCCGCTG GCTCTTTTCA GCCTCCCAAT GCTGCAAGTC AGCTCCACAG CTTTGCCTAC 960 TGGGCCAAGT GCCTCCAGGC CCCCTGCATG GCCCTCTGTC CACAGCACCA AGTGTGAGTG 1020 ACTGGGGGTC CCTCAGGGGC TGCCCCCACC AGGCTGTGCC AAGCCCTGAT CCTCAGGGAC 1080 TTCCTGGGGT GGGAATGTGG GCCTGTGAGA GTGGGAAGCC CGCCAGGAAG TTCCCAGAAC 1140 CTGGGATCCT GGTTTCCAGT GCTTGCTGGG GCCACCCTCA 1180
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