| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39349826-39350008 | Common:1; Rare:54 | ||||
| chr22:40346427-40346556 | Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40819321-40819506 | Common:11; Rare:99 | ||||
| chr22:40856584-40857159 | Common:2; Rare:224; Clinvar:3 | ||||
| chr22:40951015-40951401 | Common:2; Rare:134 | ||||
| chr22:41286155-41286428 | Common:2; Rare:84 | ||||
| chr22:41446784-41446935 | Rare:57 | ||||
| chr22:41468645-41468810 | Common:2; Rare:47 | ||||
| chr22:41468939-41469142 | Rare:55 | ||||
| chr22:41621012-41621370 | Common:7; Rare:133 | ||||
| chr22:41800540-41800683 | Common:1; Rare:42 | ||||
| chr22:41832909-41833131 | Common:3; Rare:71 | ||||
| chr22:42070779-42070935 | Common:1; Rare:32 | ||||
| chr22:42079473-42079763 | Common:2; Rare:76 | ||||
| chr22:42090730-42090902 | Common:1; Rare:65; Clinvar (pathogenic):1 |