| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446790-41446935 | Rare:54 | ||||
| chr22:41468657-41468792 | Common:2; Rare:38 | ||||
| chr22:41469053-41469144 | Rare:36 | ||||
| chr22:41560902-41561132 | Common:9; Rare:66 | ||||
| chr22:41621018-41621370 | Common:7; Rare:131 | ||||
| chr22:41800517-41800631 | Rare:37 | ||||
| chr22:41832909-41833139 | Common:3; Rare:75 | ||||
| chr22:42070782-42070948 | Common:2; Rare:33 | ||||
| chr22:42079629-42079763 | Common:1; Rare:40 | ||||
| chr22:42090607-42090960 | Common:2; Rare:149; Clinvar (pathogenic):1 | ||||
| chr22:42519782-42519874 | Common:1; Rare:40 | ||||
| chr22:42614811-42615246 | Common:4; Rare:190 | ||||
| chr22:42649322-42649482 | Common:1; Rare:64 | ||||
| chr22:43015075-43015384 | Common:2; Rare:127 | ||||
| chr22:43812208-43812441 | Common:3; Rare:78 |