| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446790-41446980 | Rare:81 | ||||
| chr22:41468617-41468813 | Common:2; Rare:52 | ||||
| chr22:41468982-41469170 | Rare:67 | ||||
| chr22:41544322-41544654 | Common:9; Rare:126 | ||||
| chr22:41560908-41561143 | Common:9; Rare:69 | ||||
| chr22:41621018-41621390 | Common:7; Rare:136 | ||||
| chr22:41800506-41800631 | Rare:40 | ||||
| chr22:41832896-41833355 | Common:3; Rare:151 | ||||
| chr22:41947122-41947261 | Rare:46 | ||||
| chr22:41976486-41976582 | Rare:19 | ||||
| chr22:41976685-41977047 | Rare:96 | ||||
| chr22:42070792-42070971 | Common:2; Rare:36 | ||||
| chr22:42079603-42079778 | Common:1; Rare:56 | ||||
| chr22:42090730-42091054 | Common:1; Rare:112; Clinvar (pathogenic):1 | ||||
| chr22:42210401-42210451 | Rare:12 |