| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106862979-106863180 | Rare:69 | ||||
| chr9:108934074-108934471 | Common:7; Rare:157; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:111038190-111038367 | Common:2; Rare:53 | ||||
| chr9:112379834-112380150 | Common:3; Rare:130 | ||||
| chr9:113221262-113221558 | Rare:91 | ||||
| chr9:113275392-113275689 | Common:4; Rare:85; Clinvar (pathogenic):1 | ||||
| chr9:113340280-113340437 | Common:2; Rare:36 | ||||
| chr9:113410276-113410705 | Common:3; Rare:127 | ||||
| chr9:120793345-120793526 | Common:1; Rare:75 | ||||
| chr9:120842905-120843031 | Common:1; Rare:45 | ||||
| chr9:121074858-121074967 | Rare:52 | ||||
| chr9:121370231-121370512 | Common:1; Rare:77 | ||||
| chr9:122159730-122159885 | Rare:53 | ||||
| chr9:122264810-122264916 | Common:1; Rare:30 | ||||
| chr9:122913305-122913377 | Common:1; Rare:17 |