| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37560343-37560525 | Common:1; Rare:67 | ||||
| chr22:37849316-37849446 | Rare:74 | ||||
| chr22:37953609-37953737 | Rare:53 | ||||
| chr22:38656363-38656741 | Common:1; Rare:98 | ||||
| chr22:38681813-38682239 | Common:3; Rare:162 | ||||
| chr22:40856824-40857126 | Common:2; Rare:109; Clinvar:1 | ||||
| chr22:41286172-41286435 | Common:2; Rare:79 | ||||
| chr22:41468633-41468827 | Common:2; Rare:55 | ||||
| chr22:41469076-41469164 | Rare:41 | ||||
| chr22:41621035-41621388 | Common:7; Rare:131 | ||||
| chr22:42090735-42090947 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
| chr22:42614853-42615244 | Common:3; Rare:159 | ||||
| chr22:42649314-42649592 | Common:6; Rare:97 | ||||
| chr22:44312859-44313040 | Common:1; Rare:37 | ||||
| chr22:45163705-45163941 | Common:4; Rare:84 |