| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:83219172-83219357 | Common:2; Rare:44 | ||||
| chr9:86348399-86348693 | Rare:60 | ||||
| chr9:94347453-94347616 | Rare:30 | ||||
| chr9:97238264-97238511 | Common:4; Rare:72 | ||||
| chr9:101424934-101425194 | Common:1; Rare:67; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr9:124658124-124658443 | Rare:59 | ||||
| chr9:129496731-129496931 | Common:2; Rare:59 | ||||
| chr9:133063234-133063294 | Rare:14 | ||||
| chr9:133064078-133064374 | Common:1; Rare:57 | ||||
| chr9:133064386-133064776 | Common:1; Rare:135; Clinvar:1 | ||||
| chr9:133066227-133066799 | Common:2; Rare:160 | ||||
| chr9:133068647-133069288 | Common:3; Rare:146; Clinvar:1 | ||||
| chr9:133071817-133072401 | Common:3; Rare:106 | ||||
| chr9:133086291-133086425 | Common:3; Rare:73 | ||||
| chr9:133086881-133087100 | Common:10; Rare:84 |