| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98119184-98119364 | Common:1; Rare:46 | ||||
| chr9:98119288-98119418 | Rare:24 | ||||
| chr9:98192586-98192876 | Common:12; Rare:158 | ||||
| chr9:98255540-98256120 | Common:6; Rare:220 | ||||
| chr9:99221865-99222369 | Common:5; Rare:399; Clinvar:8; Clinvar (benign):7 | ||||
| chr9:99906558-99906751 | Rare:159 | ||||
| chr9:100098949-100099342 | Common:7; Rare:218; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:100352828-100353114 | Rare:199 | ||||
| chr9:100426870-100427370 | Common:7; Rare:204 | ||||
| chr9:101028608-101028937 | Common:5; Rare:196 | ||||
| chr9:101398556-101399026 | Common:2; Rare:276 | ||||
| chr9:101533732-101533917 | Rare:119 | ||||
| chr9:104093976-104094358 | Common:7; Rare:193 | ||||
| chr9:104747410-104747800 | Common:2; Rare:156 | ||||
| chr9:105244261-105244752 | Common:8; Rare:267 |