| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19408782-19409012 | Common:3; Rare:91 | ||||
| chr9:20684074-20684282 | Common:3; Rare:82 | ||||
| chr9:21802513-21802696 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:26892719-26892865 | Rare:74 | ||||
| chr9:26947117-26947271 | Rare:56 | ||||
| chr9:26956315-26956464 | Common:2; Rare:54 | ||||
| chr9:27109371-27109511 | Rare:28; Clinvar (benign):1 | ||||
| chr9:27529705-27529910 | Common:5; Rare:58 | ||||
| chr9:32783384-32783649 | Common:2; Rare:69 | ||||
| chr9:33001565-33001804 | Common:3; Rare:107; Clinvar (benign):3 | ||||
| chr9:33025071-33025382 | Common:7; Rare:127 | ||||
| chr9:33076587-33076865 | Common:2; Rare:90 | ||||
| chr9:33167314-33167576 | Rare:98 | ||||
| chr9:33264932-33265147 | Rare:66 | ||||
| chr9:33290377-33290565 | Common:2; Rare:71 |