Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7012332-7012678 | Rare:119 | ||||
chr17:7931929-7932204 | Common:5; Rare:77 | ||||
chr17:10697503-10697648 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069481-14069556 | Common:2; Rare:25; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15262508-15262736 | Rare:55 | ||||
chr17:15999692-16000003 | Common:2; Rare:122; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:28335445-28335785 | Common:1; Rare:77 | ||||
chr17:28661883-28662285 | Common:1; Rare:144 | ||||
chr17:32350059-32350204 | Rare:84 | ||||
chr17:37609362-37609561 | Common:1; Rare:87 | ||||
chr17:44899393-44899741 | Common:2; Rare:105; Clinvar:2; Clinvar (benign):1 | ||||
chr17:45060993-45061332 | Common:2; Rare:89 | ||||
chr17:54968601-54968779 | Common:3; Rare:84 | ||||
chr17:59707402-59707665 | Common:3; Rare:74; Clinvar (benign):2 | ||||
chr17:63773517-63773840 | Common:2; Rare:106 |