| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127825812-127825946 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:127838443-127838686 | Rare:41 | ||||
| chr9:128094378-128094640 | Common:3; Rare:39 | ||||
| chr9:128684439-128684559 | Rare:25 | ||||
| chr9:129320875-129321013 | Rare:18 | ||||
| chr9:129413719-129413955 | Common:3; Rare:97 | ||||
| chr9:129483639-129483851 | Common:1; Rare:38 | ||||
| chr9:129488439-129488938 | Common:3; Rare:122 | ||||
| chr9:129488973-129489145 | Common:1; Rare:26 | ||||
| chr9:129495989-129496249 | Common:2; Rare:85 | ||||
| chr9:129496721-129496937 | Common:2; Rare:64 | ||||
| chr9:129607782-129607993 | Common:1; Rare:37 | ||||
| chr9:129698493-129698761 | Common:2; Rare:44 | ||||
| chr9:130712764-130713048 | Common:1; Rare:93 | ||||
| chr9:131373410-131373699 | Common:1; Rare:69 |