| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121074844-121074967 | Rare:58 | ||||
| chr9:121201829-121202028 | Common:2; Rare:60 | ||||
| chr9:121268058-121268207 | Common:1; Rare:48 | ||||
| chr9:121285867-121286107 | Common:1; Rare:41 | ||||
| chr9:121299687-121300004 | Common:2; Rare:109; Clinvar:3 | ||||
| chr9:121328886-121329315 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:121370148-121370276 | Common:1; Rare:40 | ||||
| chr9:121370278-121370404 | Common:1; Rare:24 | ||||
| chr9:122159690-122159880 | Rare:86 | ||||
| chr9:122264548-122264663 | Common:1; Rare:24 | ||||
| chr9:122264790-122264922 | Common:2; Rare:39 | ||||
| chr9:122931482-122931667 | Common:3; Rare:33 | ||||
| chr9:122940841-122941055 | Common:2; Rare:82 | ||||
| chr9:124861908-124862134 | Common:1; Rare:95 | ||||
| chr9:124940969-124941168 | Common:3; Rare:67 |