| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40177793-40178011 | Rare:61 | ||||
| chr22:40346454-40346589 | Rare:66; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr22:40405500-40405844 | Common:1; Rare:112 | ||||
| chr22:40406146-40406662 | Common:2; Rare:193 | ||||
| chr22:40463414-40463530 | Rare:21 | ||||
| chr22:40636611-40637033 | Common:2; Rare:121 | ||||
| chr22:40856419-40857169 | Common:3; Rare:306; Clinvar:4 | ||||
| chr22:40951015-40951449 | Common:2; Rare:147 | ||||
| chr22:41091404-41091846 | Common:6; Rare:165 | ||||
| chr22:41286132-41286547 | Common:2; Rare:135 | ||||
| chr22:41367190-41367465 | Rare:82 | ||||
| chr22:41446690-41446980 | Common:1; Rare:112 | ||||
| chr22:41468611-41468802 | Common:2; Rare:48 | ||||
| chr22:41468865-41469174 | Rare:90 | ||||
| chr22:41507553-41507886 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):2 |