Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:17836956-17837162 | Common:2; Rare:48 | ||||
chr17:17972375-17972623 | Common:1; Rare:76 | ||||
chr17:18039081-18039447 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18087759-18088056 | Rare:78 | ||||
chr17:18183290-18183529 | Rare:66 | ||||
chr17:18183710-18183949 | Rare:113 | ||||
chr17:18246951-18247216 | Common:8; Rare:143 | ||||
chr17:18247376-18247731 | Common:3; Rare:105 | ||||
chr17:18258177-18258343 | Rare:35 | ||||
chr17:18260411-18260691 | Rare:83 | ||||
chr17:18314870-18315368 | Common:2; Rare:138 | ||||
chr17:18315698-18315990 | Rare:94 | ||||
chr17:18363371-18363714 | Common:5; Rare:113 | ||||
chr17:18699018-18699199 | Common:1; Rare:38 | ||||
chr17:18781117-18781318 | Common:3; Rare:56 |