Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:65149280-65149419 | Rare:29 | ||||
chr1:65254349-65254544 | Common:1; Rare:73 | ||||
chr1:65419913-65420093 | Rare:43 | ||||
chr1:65420163-65420799 | Common:7; Rare:169; Clinvar:2; Clinvar (benign):1 | ||||
chr1:65420938-65421213 | Rare:56 | ||||
chr1:65992317-65992737 | Common:1; Rare:85 | ||||
chr1:65992924-65993187 | Rare:62 | ||||
chr1:66331727-66331888 | Rare:32 | ||||
chr1:66332136-66332304 | Rare:33 | ||||
chr1:66332328-66332464 | Rare:43 | ||||
chr1:66354289-66354387 | Rare:11 | ||||
chr1:66354601-66354642 | Rare:6 | ||||
chr1:66533389-66533652 | Common:2; Rare:38 | ||||
chr1:66924755-66925069 | Common:2; Rare:135 | ||||
chr1:66925112-66925422 | Common:2; Rare:106 |