Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659244-99659529 | Common:1; Rare:73 | ||||
chr10:99732056-99732356 | Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185926-100186194 | Rare:105 | ||||
chr10:100229540-100229640 | Rare:34 | ||||
chr10:100267611-100267763 | Common:2; Rare:47 | ||||
chr10:100286343-100286431 | Rare:20 | ||||
chr10:100286661-100286730 | Rare:31 | ||||
chr10:100346939-100347245 | Common:1; Rare:78 | ||||
chr10:100529794-100529972 | Rare:57 | ||||
chr10:100912655-100913023 | Common:1; Rare:108 | ||||
chr10:100913328-100913460 | Rare:33 | ||||
chr10:100987213-100987599 | Common:1; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996990-100997117 | Rare:41 | ||||
chr10:100998521-100998596 | Common:3; Rare:20 | ||||
chr10:100999633-100999924 | Common:2; Rare:88 |