| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128275900-128276302 | Common:5; Rare:176 | ||||
| chr9:128322410-128322576 | Common:1; Rare:54 | ||||
| chr9:128322739-128322866 | Common:2; Rare:49; Clinvar (benign):5 | ||||
| chr9:128371220-128371404 | Rare:71 | ||||
| chr9:128504618-128504782 | Rare:71; Clinvar:5 | ||||
| chr9:128552394-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128630042-128630339 | Common:4; Rare:74; Clinvar (benign):2 | ||||
| chr9:128632409-128632666 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):7 | ||||
| chr9:128656635-128656816 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:128683683-128683915 | Rare:60 | ||||
| chr9:128724081-128724467 | Common:2; Rare:128 | ||||
| chr9:128771847-128771966 | Rare:31 | ||||
| chr9:128787169-128787333 | Common:3; Rare:57 | ||||
| chr9:128881929-128882197 | Common:2; Rare:91 | ||||
| chr9:128922004-128922324 | Common:1; Rare:75 |