| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856434-40856735 | Rare:134 | ||||
| chr22:40856751-40857154 | Common:2; Rare:150; Clinvar:3 | ||||
| chr22:41286158-41286516 | Common:2; Rare:113 | ||||
| chr22:41446790-41446945 | Rare:60 | ||||
| chr22:41468657-41468795 | Common:2; Rare:39 | ||||
| chr22:41468980-41469159 | Rare:58 | ||||
| chr22:41621018-41621384 | Common:7; Rare:134 | ||||
| chr22:41800506-41800688 | Common:1; Rare:58 | ||||
| chr22:41832649-41832728 | Rare:14 | ||||
| chr22:41832909-41833137 | Common:3; Rare:73 | ||||
| chr22:41998602-41998803 | Common:2; Rare:71 | ||||
| chr22:42070784-42070948 | Common:2; Rare:33 | ||||
| chr22:42079517-42079771 | Common:2; Rare:70 | ||||
| chr22:42090607-42091049 | Common:2; Rare:177; Clinvar (pathogenic):1 | ||||
| chr22:42614850-42615251 | Common:3; Rare:168 |