| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19102863-19103065 | Common:2; Rare:87 | ||||
| chr9:19127455-19127616 | Common:3; Rare:50 | ||||
| chr9:19380191-19380349 | Common:4; Rare:77 | ||||
| chr9:20658235-20658359 | Common:3; Rare:51 | ||||
| chr9:20684096-20684283 | Common:3; Rare:75 | ||||
| chr9:21031586-21031700 | Common:1; Rare:50 | ||||
| chr9:26947131-26947216 | Rare:32 | ||||
| chr9:27529771-27529927 | Common:3; Rare:45 | ||||
| chr9:27573422-27573551 | Common:5; Rare:78 | ||||
| chr9:33001568-33001751 | Common:3; Rare:88; Clinvar (benign):3 | ||||
| chr9:33025071-33025357 | Common:7; Rare:121 | ||||
| chr9:33264923-33265099 | Rare:50 | ||||
| chr9:33473845-33474144 | Common:4; Rare:93 | ||||
| chr9:33817508-33817760 | Common:2; Rare:84 | ||||
| chr9:34048870-34048980 | Common:1; Rare:43 |