| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446790-41446958 | Rare:67 | ||||
| chr22:41468617-41468798 | Common:2; Rare:46 | ||||
| chr22:41469022-41469175 | Rare:63 | ||||
| chr22:41560956-41561129 | Common:8; Rare:60 | ||||
| chr22:41620992-41621398 | Common:7; Rare:148 | ||||
| chr22:41621710-41621804 | Rare:27 | ||||
| chr22:41800517-41800702 | Common:1; Rare:58 | ||||
| chr22:41832909-41833355 | Common:3; Rare:149 | ||||
| chr22:41946701-41946959 | Common:3; Rare:66 | ||||
| chr22:41947093-41947237 | Rare:55 | ||||
| chr22:42070770-42070977 | Common:3; Rare:44 | ||||
| chr22:42079513-42079823 | Common:2; Rare:92 | ||||
| chr22:42090668-42090953 | Common:2; Rare:127; Clinvar (pathogenic):1 | ||||
| chr22:42519768-42519965 | Common:1; Rare:76 | ||||
| chr22:42553728-42554003 | Common:1; Rare:84 |