| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26947131-26947267 | Rare:49 | ||||
| chr9:26947403-26947557 | Common:1; Rare:54 | ||||
| chr9:26956319-26956459 | Common:2; Rare:51 | ||||
| chr9:27529738-27529899 | Common:4; Rare:53 | ||||
| chr9:27573430-27573570 | Common:5; Rare:81 | ||||
| chr9:27573709-27573964 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32384537-32384726 | Common:1; Rare:75 | ||||
| chr9:32573051-32573338 | Common:4; Rare:97 | ||||
| chr9:33025090-33025376 | Common:7; Rare:120 | ||||
| chr9:33166880-33166956 | Rare:33 | ||||
| chr9:33264936-33265090 | Rare:44 | ||||
| chr9:33290394-33290565 | Common:2; Rare:64 | ||||
| chr9:33473877-33474144 | Common:2; Rare:77 | ||||
| chr9:34048845-34049178 | Common:2; Rare:120 | ||||
| chr9:34178821-34179081 | Common:1; Rare:67 |