| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26892482-26892828 | Common:1; Rare:170 | ||||
| chr9:26947103-26947288 | Common:1; Rare:69 | ||||
| chr9:26947444-26947561 | Common:1; Rare:33 | ||||
| chr9:27005601-27005888 | Common:2; Rare:54 | ||||
| chr9:27109053-27109243 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:27529623-27529641 | |||||
| chr9:27529709-27529799 | Common:2; Rare:26 | ||||
| chr9:27529801-27529909 | Common:3; Rare:28 | ||||
| chr9:27573430-27573551 | Common:5; Rare:75 | ||||
| chr9:27573723-27574024 | Common:4; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384478-32384729 | Common:1; Rare:91 | ||||
| chr9:32552532-32552813 | Common:2; Rare:62; Clinvar:2 | ||||
| chr9:32573041-32573283 | Common:4; Rare:89 | ||||
| chr9:33001543-33001721 | Common:2; Rare:97; Clinvar (benign):4 | ||||
| chr9:33025058-33025383 | Common:7; Rare:133 |