| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113340237-113340385 | Common:2; Rare:37 | ||||
| chr9:113376908-113377105 | Common:7; Rare:64 | ||||
| chr9:113410226-113410705 | Common:3; Rare:140 | ||||
| chr9:114387975-114388170 | Common:1; Rare:58 | ||||
| chr9:116687228-116687361 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793214-120793534 | Common:1; Rare:114 | ||||
| chr9:120842905-120843239 | Common:1; Rare:109 | ||||
| chr9:121074837-121074992 | Rare:78 | ||||
| chr9:121201814-121202149 | Common:2; Rare:105 | ||||
| chr9:121286026-121286150 | Rare:33 | ||||
| chr9:121286441-121286676 | Common:2; Rare:52 | ||||
| chr9:121299692-121299997 | Common:2; Rare:106; Clinvar:3 | ||||
| chr9:121370183-121370453 | Common:2; Rare:80 | ||||
| chr9:122159627-122159908 | Rare:117 | ||||
| chr9:122264733-122264927 | Common:2; Rare:55 |