| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41413760-41414075 | Common:2; Rare:93 | ||||
| chr22:41517341-41517589 | Common:3; Rare:64 | ||||
| chr22:41518356-41518570 | Common:3; Rare:50; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:41522775-41523216 | Rare:124; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr22:41532120-41532227 | Rare:48 | ||||
| chr22:41836555-41836744 | Common:2; Rare:31 | ||||
| chr22:42582000-42582196 | Common:4; Rare:77 | ||||
| chr22:42601201-42601229 | Rare:7 | ||||
| chr22:42856210-42856434 | Common:2; Rare:59 | ||||
| chr22:42879082-42879397 | Common:2; Rare:90 | ||||
| chr22:42903641-42903826 | Common:3; Rare:33 | ||||
| chr22:42937543-42937712 | Rare:29 | ||||
| chr22:42995164-42995494 | Rare:53 | ||||
| chr22:43003944-43004135 | Common:1; Rare:25 | ||||
| chr22:43179552-43179676 | Common:1; Rare:39 |