Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:95693856-95694180 | Common:5; Rare:111; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95907820-95907920 | Common:1; Rare:27 | ||||
chr10:96043425-96043594 | Common:1; Rare:61 | ||||
chr10:96832176-96832314 | Rare:50 | ||||
chr10:97426040-97426256 | Common:2; Rare:84 | ||||
chr10:97445961-97446232 | Common:1; Rare:75 | ||||
chr10:97498382-97498550 | Common:2; Rare:69 | ||||
chr10:98268180-98268442 | Common:3; Rare:68 | ||||
chr10:99430616-99430957 | Common:3; Rare:82 | ||||
chr10:99659256-99659579 | Common:2; Rare:81 | ||||
chr10:99732053-99732325 | Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185920-100186182 | Rare:102 | ||||
chr10:100913335-100913438 | Rare:28 | ||||
chr10:100987445-100987573 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031146-101031302 | Rare:34 |