| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40951607-40951716 | Common:1; Rare:31 | ||||
| chr22:41091391-41091749 | Common:5; Rare:127 | ||||
| chr22:41286167-41286547 | Common:2; Rare:117 | ||||
| chr22:41446795-41446980 | Rare:79 | ||||
| chr22:41468628-41468798 | Common:2; Rare:45 | ||||
| chr22:41469039-41469145 | Rare:38 | ||||
| chr22:41621006-41621352 | Common:7; Rare:129 | ||||
| chr22:41800512-41800712 | Common:1; Rare:62 | ||||
| chr22:41832798-41833149 | Common:3; Rare:110 | ||||
| chr22:41946692-41946950 | Common:3; Rare:66 | ||||
| chr22:41947089-41947243 | Rare:55 | ||||
| chr22:42070793-42070961 | Common:2; Rare:34 | ||||
| chr22:42079575-42079763 | Common:1; Rare:55 | ||||
| chr22:42090730-42091049 | Common:1; Rare:111; Clinvar (pathogenic):1 | ||||
| chr22:42519753-42519965 | Common:1; Rare:85 |