| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684101-20684292 | Common:3; Rare:78 | ||||
| chr9:21031602-21031781 | Common:1; Rare:56 | ||||
| chr9:21802549-21802692 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:22009294-22009498 | Common:1; Rare:62 | ||||
| chr9:23826298-23826493 | Common:1; Rare:77 | ||||
| chr9:26892738-26892824 | Rare:52 | ||||
| chr9:26947107-26947299 | Common:1; Rare:69 | ||||
| chr9:26947427-26947571 | Common:1; Rare:43 | ||||
| chr9:26956265-26956464 | Common:2; Rare:75 | ||||
| chr9:27573422-27573530 | Common:5; Rare:56 | ||||
| chr9:32384479-32384728 | Common:1; Rare:90 | ||||
| chr9:32552014-32552365 | Common:2; Rare:92 | ||||
| chr9:33001543-33001733 | Common:2; Rare:98; Clinvar (benign):4 | ||||
| chr9:33025066-33025432 | Common:8; Rare:146 | ||||
| chr9:33166867-33166956 | Rare:35 |