Tag | Content |
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EnhancerAtlas ID | HS184-13299 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr17:30625220-30626960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr17:30625286-30625296 | GGGGCGGGGC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGTAGGCA GGTAGGCCCC GTGTCCACAA AGGCACACTG CCCCAGGGTG GGGTGGGAGA 60 CCCTGTGGGG CGGGGCAAGC CCCAGGTTTC CAGGACACAC AGAAGATCCT CATCTCCAAG 120 GCTCCTGACT TAACCAGGCT GTCCTCCAGG CACACCCACC TCCCTATGAG GCTGGAGAAC 180 GGACTGCTGC CCATAGAGGG AGGTGTGTGG CAGGACGGGG GAGGAGAGCA CTGGATTTGG 240 GACAGGCTGG ACAACCGACT CTCGGTCTCA CACCACCATG TGGTAGCTCT CTGAGCTTGG 300 GGAAATTTCC TAACCTCTTT TGGCCATGTT AAGCTTTAAG AGGGAACTAA TGAGATCTGC 360 CTGTAGGGTT GCCAGGAGGG CAGAGTGAGT GAGGCAACAG ATGGAACAAC AGTGCTCCGA 420 AAACTGCAAG GGCACAGTGA GATCCCCACA GGGGAATCAA AGGGGTGAGT GGAGCCAGGT 480 ACCACCCTGG CCACGTAGCA CCTGTCCCCA AAAAGAGAGC TGGCTGCTAC CCAGACCAAC 540 CGCAGTCCCC TTGCCTGACC CACTGCTGAC AGGGAGTCTG ACCTAAGAGG CAGTGAGCCC 600 TGGCTCCATC TGAAGGCATC TGGGCCTCCA GCTGAGTGGG CACACGTGTG GCCAGTGATC 660 ATCCTTCATG GATAGTGGCC AGAGTGACTC CCAGTGAGCC TTCCACCTTC TGCCCCCTCC 720 CCAGTGGGAG GTGAGGTGGG TGAAGTTAGC TGGGGAGAGC ACGGATTTCT GCAGGAAGCG 780 TCTGCCAGCC AGGCCTCTGA ACATGAGGAT CTCCCTCGTG ATGTCTCCAA CTTTATTGCC 840 GGCTGTTTTT TTTTTTTTTT TTAACAAGGT TTGCCGCCTC AGCTCTTCAG CTTGACAGCT 900 GTGCCCAAGG GAGCTTTGTG TGTATGTTTA AGTAAGATCT TAATCCTTTC TGAGTGGTAT 960 TAAAGTTGTC ATCAGGAGAG CCGGGCAGCG TCAGCCTTGT AAACAACAGG CAGGCAGGGA 1020 CCCTGGGAGT AACTGAAGTG GTTTCAGAAA TCAAAGAGGA AGGGTCCCAC CCCACCCACA 1080 CGAGGCTGGT CTGCTAGTGC ATGAACCCTT GGCCTGGGAG ATTCACCCTG CACCATCTCC 1140 TTTGCTCCTG TATGCGCTGA GGTTAAAATC GTTGGCCACC TTGGTCAGCA CCCCTGCAAG 1200 CCCCTCCCAG AATCCAAGGC TCACCACGTC CTTGAATAAA GGGCTAATGA GCATCTCTAA 1260 GTGCCAGACT TGTTCAGCCA CCCACACACC CCCTAATCCT GACATCTGAG GATTGATAGC 1320 CTCATTTTCC ATACCTCAAT ACCCAGAGAC CCAGATGTTA AATAGCAAGG AACAGGGAAG 1380 ACATTAATAA CATTTGCAGT TAGTATTCAA TTAGATGGGA ATGCCAATAA CCTAGAAGAC 1440 AAAAATAAGA TTCAAATGGA CTCAGACCTC ACCCAAACCA GGTGACATGC AGTGGGGAGA 1500 CAGAGTAGGT GTCACCTCCC CAGTGACACC AGTGCAGAGT GGGAAGATTC AAACAGAAGC 1560 AGAGCTCATC ACCTGAATGT GAGCATGTAG GGCTGTATCA TTGAGCACAT GGCGTGCACT 1620 GTTCTGTCTG AGTCAGTGAT TAAGACCAGA GGGCACTCTG GTCACCACAC ATGTCATTGA 1680 TCTCCATGAT TGAGTTGATT GATCTGTCTC TGCTGTCTAC CCTTTCCTGT CCTCCCAAGC 1740
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