| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128340427-128340810 | Common:3; Rare:120 | ||||
| chr9:128371220-128371433 | Rare:84 | ||||
| chr9:128552413-128552611 | Rare:78; Clinvar:1 | ||||
| chr9:128630134-128630337 | Common:3; Rare:52; Clinvar (benign):2 | ||||
| chr9:128656629-128656921 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:128683291-128683536 | Common:4; Rare:35 | ||||
| chr9:128683616-128683898 | Rare:66 | ||||
| chr9:128684458-128684625 | Rare:40 | ||||
| chr9:128684935-128685165 | Rare:42 | ||||
| chr9:128689516-128689648 | Rare:52 | ||||
| chr9:128690984-128691245 | Common:3; Rare:89 | ||||
| chr9:128724064-128724491 | Common:5; Rare:146 | ||||
| chr9:128771854-128771980 | Rare:35 | ||||
| chr9:128772450-128772512 | Rare:9 | ||||
| chr9:128881901-128882245 | Common:2; Rare:118 |