| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16870728-16870866 | Rare:62 | ||||
| chr9:19102850-19103008 | Common:1; Rare:65 | ||||
| chr9:19380191-19380373 | Common:4; Rare:88 | ||||
| chr9:20684115-20684282 | Common:2; Rare:64 | ||||
| chr9:26892731-26892858 | Rare:67 | ||||
| chr9:26947117-26947254 | Rare:50 | ||||
| chr9:33001538-33001751 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr9:33025081-33025312 | Common:6; Rare:99 | ||||
| chr9:34048876-34048986 | Common:1; Rare:43 | ||||
| chr9:34049175-34049268 | Common:1; Rare:22 | ||||
| chr9:34178977-34179084 | Rare:32 | ||||
| chr9:34329181-34329593 | Rare:130 | ||||
| chr9:34612073-34612203 | Common:7; Rare:48 | ||||
| chr9:34652050-34652207 | Rare:46 | ||||
| chr9:35079753-35080041 | Common:5; Rare:64; Clinvar:4; Clinvar (benign):4 |