| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101533752-101533903 | Rare:46 | ||||
| chr9:104094012-104094345 | Common:2; Rare:75 | ||||
| chr9:104094514-104094603 | Common:1; Rare:30 | ||||
| chr9:104747617-104747795 | Common:1; Rare:56 | ||||
| chr9:105447953-105448144 | Common:2; Rare:68 | ||||
| chr9:105558046-105558170 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862873-106863180 | Rare:87 | ||||
| chr9:107489767-107490022 | Common:3; Rare:105 | ||||
| chr9:108934074-108934510 | Common:7; Rare:178; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498268-109498433 | Rare:55 | ||||
| chr9:110125345-110125530 | Rare:33 | ||||
| chr9:110125532-110125553 | Rare:6 | ||||
| chr9:110256410-110256703 | Common:4; Rare:102 | ||||
| chr9:110579879-110580040 | Common:1; Rare:42 | ||||
| chr9:111037441-111037648 | Rare:30 |