| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446663-41446980 | Common:1; Rare:116 | ||||
| chr22:41468649-41468751 | Common:2; Rare:33 | ||||
| chr22:41468949-41469358 | Common:1; Rare:146 | ||||
| chr22:41620960-41621384 | Common:7; Rare:149 | ||||
| chr22:41800517-41800710 | Common:1; Rare:59 | ||||
| chr22:41832637-41832720 | Rare:16 | ||||
| chr22:41832849-41833291 | Common:3; Rare:156 | ||||
| chr22:41940198-41940382 | Common:1; Rare:38 | ||||
| chr22:42070770-42071049 | Common:3; Rare:64 | ||||
| chr22:42074129-42074301 | Common:2; Rare:35 | ||||
| chr22:42079488-42079763 | Common:2; Rare:72 | ||||
| chr22:42090607-42090630 | Rare:6 | ||||
| chr22:42090658-42091144 | Common:2; Rare:190; Clinvar (pathogenic):1 | ||||
| chr22:42519782-42520119 | Common:2; Rare:103 | ||||
| chr22:42614816-42615416 | Common:6; Rare:366 |