| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:124354281-124354483 | Rare:37 | ||||
| chr9:124354719-124355016 | Common:1; Rare:63 | ||||
| chr9:124355209-124355486 | Common:2; Rare:65 | ||||
| chr9:124357536-124357727 | Rare:33 | ||||
| chr9:124357836-124358136 | Rare:70 | ||||
| chr9:124658391-124658436 | Rare:9 | ||||
| chr9:124669466-124669660 | Rare:40 | ||||
| chr9:127447968-127448114 | Rare:36 | ||||
| chr9:127482739-127483011 | Rare:55; Clinvar:2 | ||||
| chr9:127816044-127816129 | Common:1; Rare:25; Clinvar:1 | ||||
| chr9:127818123-127818565 | Common:1; Rare:121; Clinvar:7; Clinvar (benign):8 | ||||
| chr9:127819625-127819719 | Rare:29; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:127838491-127838615 | Rare:24 | ||||
| chr9:128094430-128094637 | Common:3; Rare:30 | ||||
| chr9:128258022-128258439 | Common:2; Rare:114 |