| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100098964-100099336 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352831-100353013 | Rare:64 | ||||
| chr9:101398511-101398906 | Common:1; Rare:140 | ||||
| chr9:104747639-104747795 | Common:1; Rare:48 | ||||
| chr9:104763859-104764215 | Common:2; Rare:69 | ||||
| chr9:105558019-105558159 | Rare:49; Clinvar (benign):1 | ||||
| chr9:106863001-106863180 | Rare:62 | ||||
| chr9:107489767-107490058 | Common:4; Rare:126 | ||||
| chr9:108934074-108934493 | Common:7; Rare:169; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109119483-109119560 | Common:1; Rare:31 | ||||
| chr9:109498235-109498433 | Rare:65 | ||||
| chr9:110256416-110256703 | Common:4; Rare:102 | ||||
| chr9:110580029-110580098 | Rare:9 | ||||
| chr9:111038717-111038916 | Common:4; Rare:54 | ||||
| chr9:111631160-111631515 | Common:2; Rare:104 |