Tag | Content |
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EnhancerAtlas ID | HS156-06245 | Organism | Homo sapiens | Tissue/cell | P493-6 | Coordinate | chr19:17306280-17306960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr19:17306289-17306300 | CCACACCCTCT | + | 6.02 | ZNF263 | MA0528.1 | chr19:17306921-17306942 | GAGGGAGAGAGAGAGAGAGGG | + | 6.32 | ZNF263 | MA0528.1 | chr19:17306905-17306926 | GATGGATGGAGGGAGGGAGGG | + | 6.43 | ZNF263 | MA0528.1 | chr19:17306917-17306938 | GAGGGAGGGAGAGAGAGAGAG | + | 6.89 | ZNF263 | MA0528.1 | chr19:17306913-17306934 | GAGGGAGGGAGGGAGAGAGAG | + | 6.9 | ZNF263 | MA0528.1 | chr19:17306909-17306930 | GATGGAGGGAGGGAGGGAGAG | + | 7 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGTAAGCCC CACACCCTCT TTTGTCTGAG CACCAGGGTC CAGGCCAGGT GGGCAAGGCC 60 AGGGGCAGTG CCACACATCC TGGAAACACA TGTGTAATCA TGCCCAGTGG GTGTGCGGGA 120 GGCCTGAGGG AGGAGGACGA GCAGGACATG CTAAAGACCA AGTGAAGACA AGGCAGCCAG 180 CCAGGGCCCA GGCTGGGACC TGGAGCCTTG AGGGGTCCCC AGAAGGAGCT GTGCTCACAC 240 AGAAAGGCCC CGGCCTTGAG AGAGGTGGCT CCTCAGGTCA AGGTCCCTGC TGCCCAGAAA 300 TCTTGGGCCT TGGTTTCTAA TTGGTGAACA GGACTAACTG CACTCCTCGG GGTTAAAGGA 360 GCAGGGGCTT GCTCTGCCTG AGCCTTAGTA AGCCAAGTGT CAGTGACTTG GAATCTCCAG 420 CTCCCTCTTC CAGAGGGCCT GCAGGACCAA AGGAAAGAAA TCAGGGAGGA GACAGGCCTT 480 CCCTGCAGCA GGCCTGCTCA GCCTCCCACT GCTCGTATTG GGGGCCAGAT CATTCTCTGC 540 GGTGGGGGCT GTCCTGTGTA TCATAAGATG TTGAGCAGCA TCCCTGGCCT CCACTTACCA 600 CATGCCAGGA GTATTATCGA TAGATGATGG ATGGAGGGAG GGAGGGAGAG AGAGAGAGAG 660 GGAAGGATGT GTGGGTGGGT 680
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