| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26892738-26892865 | Rare:66 | ||||
| chr9:26947139-26947557 | Common:1; Rare:140 | ||||
| chr9:26956295-26956472 | Common:2; Rare:63 | ||||
| chr9:27529732-27529899 | Common:5; Rare:53 | ||||
| chr9:27573414-27573562 | Common:6; Rare:87 | ||||
| chr9:27573723-27573961 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32526197-32526342 | Common:3; Rare:30 | ||||
| chr9:32552108-32552351 | Common:2; Rare:72 | ||||
| chr9:32552557-32552655 | Common:1; Rare:18; Clinvar:2 | ||||
| chr9:32573005-32573203 | Common:2; Rare:68 | ||||
| chr9:33001542-33001757 | Common:3; Rare:104; Clinvar (benign):4 | ||||
| chr9:33025081-33025383 | Common:7; Rare:125 | ||||
| chr9:33025733-33025881 | Rare:57 | ||||
| chr9:33076587-33076757 | Common:2; Rare:61 | ||||
| chr9:33264932-33265094 | Rare:45 |