| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127787951-127788270 | Common:2; Rare:104 | ||||
| chr9:127802719-127803032 | Common:3; Rare:86 | ||||
| chr9:127897338-127897536 | Common:1; Rare:42 | ||||
| chr9:127937832-127938156 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:128098278-128098545 | Common:1; Rare:55 | ||||
| chr9:128098745-128099065 | Common:2; Rare:73 | ||||
| chr9:128191438-128191642 | Rare:63 | ||||
| chr9:128191753-128191804 | Common:1; Rare:13 | ||||
| chr9:128191806-128191836 | Rare:6 | ||||
| chr9:128275914-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322729-128322880 | Common:2; Rare:68; Clinvar (benign):5 | ||||
| chr9:128340456-128340738 | Common:2; Rare:89 | ||||
| chr9:128371225-128371401 | Rare:66 | ||||
| chr9:128552388-128552611 | Rare:82; Clinvar:1 |