| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107637719-107638013 | Common:1; Rare:68 | ||||
| chr9:113620591-113620722 | Common:1; Rare:27 | ||||
| chr9:114397930-114398145 | Rare:41 | ||||
| chr9:114398452-114398632 | Common:1; Rare:42 | ||||
| chr9:121499720-121499853 | Rare:40 | ||||
| chr9:125538247-125538287 | Rare:3 | ||||
| chr9:127447968-127448059 | Rare:23 | ||||
| chr9:127566750-127566998 | Common:2; Rare:38 | ||||
| chr9:127810770-127810978 | Rare:41 | ||||
| chr9:127815952-127816136 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127825818-127826130 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr9:128094374-128094638 | Common:3; Rare:39 | ||||
| chr9:129174934-129175006 | Rare:15 | ||||
| chr9:129175896-129176098 | Common:2; Rare:61 | ||||
| chr9:129320822-129321013 | Rare:30 |