| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101398580-101398898 | Common:1; Rare:107 | ||||
| chr9:101487086-101487409 | Common:3; Rare:69 | ||||
| chr9:104093985-104094321 | Common:3; Rare:78 | ||||
| chr9:104747559-104747767 | Rare:56 | ||||
| chr9:106862979-106863172 | Rare:66 | ||||
| chr9:108934065-108934493 | Common:7; Rare:170; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498244-109498457 | Rare:69 | ||||
| chr9:110207515-110207563 | Rare:14 | ||||
| chr9:110256431-110256725 | Common:5; Rare:106 | ||||
| chr9:112333482-112333968 | Common:1; Rare:144 | ||||
| chr9:112379800-112380150 | Common:3; Rare:141 | ||||
| chr9:112718027-112718150 | Common:2; Rare:33 | ||||
| chr9:113056657-113056924 | Common:1; Rare:86; Clinvar:1 | ||||
| chr9:113221251-113221649 | Common:1; Rare:121 | ||||
| chr9:113275397-113275734 | Common:5; Rare:112; Clinvar (pathogenic):1 |