| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41620880-41621433 | Common:8; Rare:191 | ||||
| chr22:41800536-41800691 | Common:1; Rare:48 | ||||
| chr22:41832909-41833334 | Common:3; Rare:145 | ||||
| chr22:41947093-41947204 | Rare:41 | ||||
| chr22:41976456-41976582 | Rare:24 | ||||
| chr22:41976920-41977073 | Rare:44 | ||||
| chr22:41998595-41998799 | Common:2; Rare:71 | ||||
| chr22:42070782-42070971 | Common:2; Rare:38 | ||||
| chr22:42079623-42079832 | Common:1; Rare:73 | ||||
| chr22:42090607-42091073 | Common:2; Rare:181; Clinvar (pathogenic):1 | ||||
| chr22:42210637-42211042 | Common:1; Rare:118 | ||||
| chr22:42519782-42519899 | Common:1; Rare:47 | ||||
| chr22:42553719-42553928 | Common:1; Rare:62 | ||||
| chr22:42614853-42615244 | Common:3; Rare:159 | ||||
| chr22:42649322-42649495 | Common:1; Rare:71 |