Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:22451781-22451879 | Rare:38 | ||||
chr1:23559359-23559648 | Common:1; Rare:123 | ||||
chr1:23800732-23800959 | Common:1; Rare:80 | ||||
chr1:23959641-23959854 | Common:2; Rare:57 | ||||
chr1:24556022-24556149 | Common:2; Rare:37 | ||||
chr1:25232448-25232645 | Rare:79 | ||||
chr1:25247431-25247642 | Common:2; Rare:79 | ||||
chr1:25338190-25338447 | Common:1; Rare:91 | ||||
chr1:25819885-25820029 | Common:3; Rare:44 | ||||
chr1:26279824-26280127 | Rare:154 | ||||
chr1:26432112-26432404 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472247-26472523 | Common:4; Rare:87 | ||||
chr1:26900451-26900471 | Rare:8 | ||||
chr1:26921529-26921804 | Common:3; Rare:83 | ||||
chr1:27772953-27773269 | Common:1; Rare:102 |