| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:89310877-89311200 | Common:3; Rare:100 | ||||
| chr9:92115378-92115492 | Common:1; Rare:31; Clinvar:1 | ||||
| chr9:92293660-92293880 | Common:3; Rare:75 | ||||
| chr9:92325301-92325645 | Common:5; Rare:80 | ||||
| chr9:93451469-93451895 | Common:3; Rare:125 | ||||
| chr9:96383636-96383777 | Common:1; Rare:45 | ||||
| chr9:96566778-96567037 | Common:1; Rare:73 | ||||
| chr9:97412006-97412189 | Common:3; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:97633347-97633829 | Common:6; Rare:149 | ||||
| chr9:97922491-97922568 | Common:2; Rare:35 | ||||
| chr9:99221906-99222354 | Common:2; Rare:174; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906597-99906694 | Rare:50 | ||||
| chr9:100098908-100099242 | Common:2; Rare:93 | ||||
| chr9:100352913-100353078 | Rare:49 | ||||
| chr9:101398612-101398890 | Common:1; Rare:85 |