| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19127369-19127629 | Common:4; Rare:79 | ||||
| chr9:19230346-19230858 | Common:8; Rare:216 | ||||
| chr9:19380160-19380383 | Common:6; Rare:114 | ||||
| chr9:19408756-19409048 | Common:5; Rare:113 | ||||
| chr9:20622452-20622710 | Rare:84 | ||||
| chr9:20683969-20684283 | Common:5; Rare:112 | ||||
| chr9:21335320-21335435 | Common:4; Rare:43 | ||||
| chr9:21994344-21994598 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:22009233-22009475 | Common:1; Rare:79 | ||||
| chr9:26947132-26947289 | Rare:57 | ||||
| chr9:26947421-26947563 | Common:1; Rare:45 | ||||
| chr9:26956293-26956464 | Common:2; Rare:61 | ||||
| chr9:27573717-27573972 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384537-32384732 | Common:1; Rare:77 | ||||
| chr9:33025049-33025383 | Common:7; Rare:135 |