| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906591-99906684 | Rare:43 | ||||
| chr9:100098972-100099268 | Common:2; Rare:78 | ||||
| chr9:100352860-100353071 | Rare:72 | ||||
| chr9:101398582-101398887 | Common:1; Rare:101 | ||||
| chr9:104747583-104747700 | Rare:27 | ||||
| chr9:109498268-109498379 | Rare:36 | ||||
| chr9:112379848-112380134 | Common:2; Rare:118 | ||||
| chr9:113221257-113221574 | Common:1; Rare:98 | ||||
| chr9:113275403-113275728 | Common:5; Rare:110; Clinvar (pathogenic):1 | ||||
| chr9:113410394-113410775 | Common:3; Rare:110 | ||||
| chr9:114587415-114587809 | Common:3; Rare:134 | ||||
| chr9:120580135-120580360 | Common:1; Rare:74; Clinvar:3 | ||||
| chr9:120793381-120793542 | Common:1; Rare:60 | ||||
| chr9:120877157-120877512 | Common:3; Rare:123 | ||||
| chr9:121074849-121074967 | Rare:57 |