| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19380184-19380349 | Common:4; Rare:79 | ||||
| chr9:20684074-20684282 | Common:3; Rare:82 | ||||
| chr9:21802515-21802700 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:22009211-22009478 | Common:1; Rare:87 | ||||
| chr9:26892734-26892887 | Common:1; Rare:77 | ||||
| chr9:26947127-26947294 | Rare:60 | ||||
| chr9:26956265-26956470 | Common:2; Rare:77 | ||||
| chr9:27529738-27529910 | Common:4; Rare:55 | ||||
| chr9:27573422-27573535 | Common:5; Rare:61 | ||||
| chr9:27573729-27573972 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384512-32384724 | Common:1; Rare:81 | ||||
| chr9:32552556-32552649 | Common:1; Rare:17; Clinvar:2 | ||||
| chr9:32573053-32573218 | Common:2; Rare:62 | ||||
| chr9:33025052-33025397 | Common:7; Rare:137 | ||||
| chr9:33076610-33076846 | Common:2; Rare:82 |