Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15262493-15262689 | Rare:49 | ||||
chr17:15699500-15699768 | Common:3; Rare:69 | ||||
chr17:15999579-16000003 | Common:3; Rare:185; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16215532-16215606 | Rare:29 | ||||
chr17:17496392-17496513 | Rare:30 | ||||
chr17:17591587-17591926 | Common:2; Rare:96 | ||||
chr17:18314928-18315297 | Common:1; Rare:106 | ||||
chr17:18856161-18856372 | Common:1; Rare:40 | ||||
chr17:19362698-19362804 | Rare:50 | ||||
chr17:19648627-19648961 | Common:3; Rare:111 | ||||
chr17:19977807-19977925 | Common:1; Rare:41 | ||||
chr17:21214148-21214344 | Common:2; Rare:87 | ||||
chr17:27293970-27294117 | Common:1; Rare:61 | ||||
chr17:27294272-27294334 | Common:1; Rare:15 | ||||
chr17:28335377-28335832 | Common:1; Rare:110 |