| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:105558036-105558189 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862942-106863186 | Rare:78 | ||||
| chr9:108934029-108934493 | Common:7; Rare:183; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498227-109498484 | Common:1; Rare:78 | ||||
| chr9:110048509-110048718 | Common:1; Rare:60 | ||||
| chr9:110125345-110125576 | Rare:45 | ||||
| chr9:110256419-110256718 | Common:4; Rare:105 | ||||
| chr9:111038183-111038368 | Common:2; Rare:55 | ||||
| chr9:111525092-111525237 | Common:4; Rare:51 | ||||
| chr9:111599366-111599464 | Common:2; Rare:23 | ||||
| chr9:111599623-111599882 | Common:2; Rare:71 | ||||
| chr9:111661486-111661698 | Common:3; Rare:59 | ||||
| chr9:112333473-112333938 | Rare:134 | ||||
| chr9:112379753-112380157 | Common:4; Rare:153 | ||||
| chr9:112718002-112718160 | Common:2; Rare:39 |