Tag | Content |
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EnhancerAtlas ID | HS111-01922 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr16:50186940-50187650 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr16:50187061-50187072 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr16:50187134-50187144 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr16:50187062-50187072 | GGGGCGGGGC | - | 6.02 | ZNF263 | MA0528.1 | chr16:50187291-50187312 | AGGGGCGGAGGGAGGGGGGGA | + | 6.14 | ZNF263 | MA0528.1 | chr16:50187294-50187315 | GGCGGAGGGAGGGGGGGAGGG | + | 6.33 | ZNF740 | MA0753.2 | chr16:50187096-50187109 | GGGGGGGGGGCGG | - | 6.64 | ZNF740 | MA0753.2 | chr16:50187092-50187105 | GTGGGGGGGGGGG | - | 6.92 | Zfx | MA0146.2 | chr16:50187004-50187018 | CGCGCCGCGGCCTC | + | 6.28 |
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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 | CAGGTACGTG GGAGCACTCC ACAGATGGCG CAAGTACGGT TGGGCCAGGC GGTTGCGGCC 60 CCGTCGCGCC GCGGCCTCTG TGACGCACGG CGAGGCCTCC CGGGCTGCTG CGCGGCGCAG 120 CGGGGGCGGG GCGAGCGCGT GAGGGCGGGG CGGTGGGGGG GGGGGGCGGA GCGAGAGGGG 180 CGGAGCCGGC AGAGGCCCCG CCCCGGGGCC GGAGGAGCGA GGACGCTACG GAGCAGGCGC 240 GTCTCGCTGC CGCCGCTGCC GCCGCCGCCG CTCGCTCTTC TGTGGAGCCG CCGCCGCCGC 300 CGCCGCCATT TGCACGGGGA CCCCAGTGAC AGGGGCTCGG CGGAGGGGCG GAGGGGCGGA 360 GGGAGGGGGG GAGGGCCCGC GGAGCCCCCG AGGGCGGGAG CGACGCCGCC GGCGCCGGCC 420 GGGCTCCCTG CGCGACCGCG CCGCCCGCGG CGGGCCCCGA GCAGCAGCAG CAGCAGCAGC 480 GGCAGCAGCG GCAGCAGCAG CAGCAGCCGA GGCCGGGCGT GCGCCTGAGG CGGCGGCGGC 540 GGCGGCCCTG CGGGCGGCCG GGAGGGGCGG GGGCAGCGGC CGCCGCCGTT TGATGGATCC 600 GAGGATCGCC TGGTTTCAGC CAGAGCAGCT CGGACCGTCC AACAGTCTGT GGATGCAGAT 660 CTGGGAGACG ACCCAGGGGC TGAGGAACCT CTACTTCAAC CACCACTGTC 710
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