| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41468954-41469175 | Rare:77 | ||||
| chr22:41560778-41560869 | Rare:20 | ||||
| chr22:41560877-41561178 | Common:9; Rare:82 | ||||
| chr22:41621006-41621368 | Common:7; Rare:134 | ||||
| chr22:41832840-41833300 | Common:3; Rare:161 | ||||
| chr22:42090617-42091060 | Common:2; Rare:177; Clinvar (pathogenic):1 | ||||
| chr22:42614858-42615244 | Common:3; Rare:158 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42857178-42857452 | Common:3; Rare:115 | ||||
| chr22:43999045-43999320 | Common:1; Rare:52 | ||||
| chr22:44024125-44024406 | Common:2; Rare:87 | ||||
| chr22:45163766-45164008 | Common:2; Rare:93 | ||||
| chr22:46053794-46053908 | Rare:40 | ||||
| chr22:46250227-46250400 | Common:2; Rare:45 | ||||
| chr22:46267832-46268037 | Common:1; Rare:62 |