| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37592528-37592637 | Common:2; Rare:45 | ||||
| chr9:37785006-37785150 | Common:2; Rare:131; Clinvar:2; Clinvar (benign):6 | ||||
| chr9:37800673-37800945 | Common:3; Rare:182 | ||||
| chr9:37904024-37904237 | Common:2; Rare:114 | ||||
| chr9:38069029-38069449 | Common:9; Rare:234 | ||||
| chr9:38069660-38069990 | Common:4; Rare:137 | ||||
| chr9:38392504-38392807 | Common:4; Rare:161 | ||||
| chr9:38620515-38620797 | Common:2; Rare:142 | ||||
| chr9:65675927-65676793 | Common:7; Rare:156 | ||||
| chr9:68705115-68705275 | Common:1; Rare:46 | ||||
| chr9:68705417-68705812 | Common:4; Rare:198 | ||||
| chr9:68739770-68740280 | Common:5; Rare:128 | ||||
| chr9:68779907-68780107 | Common:5; Rare:139 | ||||
| chr9:69120761-69121062 | Common:5; Rare:109 | ||||
| chr9:69121087-69121631 | Common:4; Rare:231 |