| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111631135-111631304 | Rare:32 | ||||
| chr9:111661487-111661686 | Common:3; Rare:57 | ||||
| chr9:112379800-112380150 | Common:3; Rare:141 | ||||
| chr9:112718061-112718159 | Rare:23 | ||||
| chr9:113221197-113221633 | Common:1; Rare:144 | ||||
| chr9:113275397-113275734 | Common:5; Rare:112; Clinvar (pathogenic):1 | ||||
| chr9:113401233-113401430 | Common:6; Rare:84; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410197-113410692 | Common:2; Rare:153 | ||||
| chr9:114098428-114098513 | Common:5; Rare:18 | ||||
| chr9:114505410-114505545 | Common:1; Rare:43 | ||||
| chr9:116687235-116687352 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:120580118-120580366 | Common:1; Rare:80; Clinvar:5 | ||||
| chr9:120793248-120793538 | Common:2; Rare:107 | ||||
| chr9:120842905-120843099 | Common:1; Rare:68 | ||||
| chr9:120868827-120869098 | Common:2; Rare:58 |