| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39502140-39502379 | Rare:66 | ||||
| chr22:39521045-39521191 | Common:2; Rare:52 | ||||
| chr22:40044175-40044334 | Common:2; Rare:30 | ||||
| chr22:40346441-40346556 | Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40856434-40857159 | Common:2; Rare:295; Clinvar:3 | ||||
| chr22:41286175-41286432 | Common:2; Rare:76 | ||||
| chr22:41468667-41468798 | Common:2; Rare:35 | ||||
| chr22:41469008-41469159 | Rare:55 | ||||
| chr22:41621046-41621370 | Common:7; Rare:117 | ||||
| chr22:41800506-41800688 | Common:1; Rare:58 | ||||
| chr22:41832909-41833149 | Common:3; Rare:80 | ||||
| chr22:42070770-42070961 | Common:2; Rare:41 | ||||
| chr22:42074193-42074301 | Common:2; Rare:23 | ||||
| chr22:42079523-42079817 | Common:2; Rare:87 | ||||
| chr22:42090675-42090967 | Common:2; Rare:128; Clinvar (pathogenic):1 |