| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40346441-40346577 | Rare:60; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636670-40637012 | Common:2; Rare:95 | ||||
| chr22:40856939-40857150 | Common:1; Rare:85; Clinvar:3 | ||||
| chr22:41286161-41286424 | Common:2; Rare:81 | ||||
| chr22:41468466-41468769 | Common:2; Rare:83 | ||||
| chr22:41468982-41469185 | Rare:72 | ||||
| chr22:41621009-41621390 | Common:7; Rare:138 | ||||
| chr22:41947081-41947203 | Common:1; Rare:44 | ||||
| chr22:42070779-42070961 | Common:2; Rare:38 | ||||
| chr22:42090732-42090956 | Common:1; Rare:81; Clinvar (pathogenic):1 | ||||
| chr22:42614825-42615244 | Common:3; Rare:179 | ||||
| chr22:42649319-42649593 | Common:6; Rare:97 | ||||
| chr22:45163771-45163937 | Common:2; Rare:58 | ||||
| chr22:46053778-46053864 | Rare:32 | ||||
| chr22:46250245-46250404 | Common:2; Rare:47 |