Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99430586-99430930 | Common:4; Rare:80 | ||||
chr10:99659244-99659571 | Common:2; Rare:84 | ||||
chr10:99732070-99732329 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185938-100186152 | Rare:80 | ||||
chr10:100346920-100347468 | Common:3; Rare:126 | ||||
chr10:100535874-100535973 | Common:5; Rare:56 | ||||
chr10:100912741-100913040 | Common:1; Rare:94 | ||||
chr10:100987091-100987602 | Common:1; Rare:186; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996990-100997132 | Rare:41 | ||||
chr10:101031102-101031292 | Common:1; Rare:43 | ||||
chr10:101588150-101588336 | Rare:76 | ||||
chr10:101818376-101818781 | Common:1; Rare:107 | ||||
chr10:102056100-102056376 | Common:1; Rare:68 | ||||
chr10:102111262-102111493 | Rare:64 | ||||
chr10:102114944-102115061 | Common:1; Rare:41 |