| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43427443-43427572 | Rare:34 | ||||
| chr6:43427783-43427902 | Rare:29 | ||||
| chr6:43477433-43477597 | Rare:34 | ||||
| chr6:43516782-43517123 | Common:6; Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576227 | Common:1; Rare:109; Clinvar:8 | ||||
| chr6:43629158-43629484 | Common:2; Rare:92 | ||||
| chr6:43687698-43687845 | Common:1; Rare:59 | ||||
| chr6:43770087-43770222 | Common:2; Rare:40 | ||||
| chr6:43771834-43772026 | Rare:33 | ||||
| chr6:44126856-44126933 | Rare:21 | ||||
| chr6:44127278-44127669 | Common:4; Rare:108 | ||||
| chr6:44219496-44219725 | Common:2; Rare:60 | ||||
| chr6:44223489-44223830 | Common:2; Rare:106 | ||||
| chr6:44226879-44227076 | Common:3; Rare:43 | ||||
| chr6:44229437-44229737 | Rare:86 |