Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25998128-25998409 | Common:2; Rare:77 | ||||
chr1:26110898-26111246 | Common:3; Rare:105 | ||||
chr1:26234003-26234239 | Common:1; Rare:81 | ||||
chr1:26279934-26280199 | Rare:143 | ||||
chr1:26432073-26432452 | Common:5; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472304-26472627 | Common:4; Rare:120 | ||||
chr1:26695719-26696047 | Common:1; Rare:106 | ||||
chr1:26787859-26788013 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890193-26890407 | Common:1; Rare:90 | ||||
chr1:26900428-26900568 | Rare:45 | ||||
chr1:26921528-26921923 | Common:3; Rare:123 | ||||
chr1:27322020-27322338 | Common:1; Rare:114 | ||||
chr1:27392438-27392669 | Common:2; Rare:74 | ||||
chr1:27725762-27725996 | Common:2; Rare:62 | ||||
chr1:27772894-27773352 | Common:1; Rare:149 |