| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:110148550-110148662 | Common:1; Rare:18 | ||||
| chr9:111631181-111631369 | Common:1; Rare:52 | ||||
| chr9:112379873-112380140 | Common:1; Rare:114 | ||||
| chr9:113221242-113221570 | Common:1; Rare:102 | ||||
| chr9:113275397-113275694 | Common:5; Rare:87; Clinvar (pathogenic):1 | ||||
| chr9:113410315-113410686 | Common:2; Rare:107 | ||||
| chr9:114505447-114505718 | Common:2; Rare:79 | ||||
| chr9:114587457-114587583 | Common:2; Rare:43 | ||||
| chr9:114587598-114587923 | Common:2; Rare:120 | ||||
| chr9:114930509-114930691 | Common:3; Rare:47 | ||||
| chr9:116687064-116687355 | Common:5; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793373-120793475 | Rare:37 | ||||
| chr9:120842917-120843137 | Common:1; Rare:77 | ||||
| chr9:120877182-120877482 | Common:1; Rare:99 | ||||
| chr9:121074856-121074977 | Rare:59 |