Tag | Content |
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EnhancerAtlas ID | HS183-12354 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr8:144697080-144698270 | 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 | TTCCTCTGCA GGGGTGAGGC GGGGACAGTT CAGGCTCCCC AGGCCAGATC CCAGCCCTTA 60 CCTGCTCCTC CAGACGCAGA AGTGGAGACA CACCCTGGCC CTTCAGCCCT GGGAGGACCC 120 AAGCCTGCCC ATCCTAACCG TTTCCGGACA AGGCAGTGGG CTTACAGACA CCATTGCTCT 180 CCAGCCCCAC CAAGGCTGGA GGAGGGGCTG GCTCTGCCTT CCACTATGAG GAGAACCACA 240 CCCCCAGCTC AGGGCTGGGC CCCACCCAGG AGGCTGCTGA GGTCAGGGCA TAGGACCCCA 300 CTGGAGGCTG GGAAGGAGCC CAGTCTGGCC CTGGGCTGGG CTGGGGCTCC CACTACACGG 360 GGAACAGGGC GGTCTACTTC CCCACCCTGG AGGAGCTCCC ACCTGGCTCT ACTTCCCAGG 420 ATCAATGGAG CCTGCGCTTG CCGGGTCCAC CCCGCGGGCC CCACTTCCCG TGCATGAACT 480 AGACACGGCA TGGCTGGAGC CCTGGGACTG GTCTTGGGAG AAGGGAGAGG TGGTGGCCAG 540 GCAGCCTGCT GGGAAGGCCG AGACACCGAC AAAGAGGGCT CTGGGGTGAC AGGGCTCCTG 600 GGCAGAATCT CCTCTGAGCC TCTGCTCACG CTAGTGCCTC CTACGCTTAG CAAAGCCAGC 660 TAAGGCAAGG CTGCTGCCCA GTGACTGGTG GGGCCAACCC TCCGGAACAC AGCTAGCCAC 720 GGCAGGGCCC TTACACCACG CCCCCTTCCC CCAGACACAG GCAGCAGATG CACAGAGCGC 780 GGTTCACACC CCTGCACCCC AGAGTGTGTG GTGGGCCCGG CTAAGGGGAG CTGGGCCAGC 840 ACAGTCCTGG GAGCCAGAGG CTCCAGAGGC CCTGGGGACT CAGGGGGCAG GAACCAGCTC 900 CCAGTCCCAC GTGGCCGCTG GCTCTTTTCA GCCTCCCAAT GCTGCAAGTC AGCTCCACAG 960 CTTTGCCTAC TGGGCCAAGT GCCTCCAGGC CCCCTGCATG GCCCTCTGTC CACAGCACCA 1020 AGTGTGAGTG ACTGGGGGTC CCTCAGGGGC TGCCCCCACC AGGCTGTGCC AAGCCCTGAT 1080 CCTCAGGGAC TTCCTGGGGT GGGAATGTGG GCCTGTGAGA GTGGGAAGCC CGCCAGGAAG 1140 TTCCCAGAAC CTGGGATCCT GGTTTCCAGT GCTTGCTGGG GCCACCCTCA 1190
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