| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104094013-104094327 | Common:2; Rare:67 | ||||
| chr9:105447946-105448205 | Common:2; Rare:98 | ||||
| chr9:105558009-105558184 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862576-106862676 | Common:1; Rare:30 | ||||
| chr9:106862896-106863198 | Rare:89 | ||||
| chr9:107283369-107283692 | Common:3; Rare:79 | ||||
| chr9:107284035-107284180 | Common:1; Rare:33 | ||||
| chr9:108933870-108934510 | Common:10; Rare:246; Clinvar:7; Clinvar (benign):5 | ||||
| chr9:109780314-109780369 | Rare:13 | ||||
| chr9:110048530-110048858 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr9:110125297-110125581 | Rare:61 | ||||
| chr9:110256413-110256720 | Common:4; Rare:108 | ||||
| chr9:110579115-110579331 | Rare:59 | ||||
| chr9:110579494-110579652 | Common:1; Rare:44 | ||||
| chr9:110579677-110579747 | Rare:18 |