Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26244573-26244983 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):9 | ||||
chr2:26345789-26346156 | Common:1; Rare:109 | ||||
chr2:26764210-26764347 | Common:1; Rare:53 | ||||
chr2:27032852-27033004 | Rare:61 | ||||
chr2:27051546-27051696 | Rare:43 | ||||
chr2:27071532-27071884 | Common:1; Rare:109 | ||||
chr2:27078396-27078768 | Common:3; Rare:94 | ||||
chr2:27211794-27212109 | Common:3; Rare:106 | ||||
chr2:27212233-27212387 | Common:2; Rare:82 | ||||
chr2:27323058-27323154 | Rare:23 | ||||
chr2:27356746-27356854 | Rare:26 | ||||
chr2:27356942-27357191 | Common:2; Rare:90 | ||||
chr2:27370282-27370641 | Common:1; Rare:149 | ||||
chr2:27489643-27489975 | Common:1; Rare:87; Clinvar (benign):1 | ||||
chr2:27582797-27583101 | Rare:103 |