| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104928086-104928337 | Common:5; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:105447982-105448181 | Common:2; Rare:72 | ||||
| chr9:105558079-105558170 | Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:107282962-107283318 | Common:2; Rare:125 | ||||
| chr9:108889846-108890091 | Common:1; Rare:45 | ||||
| chr9:108933913-108934012 | Common:2; Rare:36; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:108934042-108934493 | Common:7; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109107975-109108228 | Common:1; Rare:46 | ||||
| chr9:109119498-109119569 | Common:1; Rare:31 | ||||
| chr9:109498237-109498484 | Common:1; Rare:74 | ||||
| chr9:110125345-110125509 | Rare:29 | ||||
| chr9:110256410-110256725 | Common:5; Rare:109 | ||||
| chr9:111599608-111599897 | Common:2; Rare:82 | ||||
| chr9:111631137-111631369 | Common:1; Rare:64 | ||||
| chr9:111661484-111661698 | Common:3; Rare:59 |