| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:14693246-14693355 | Common:1; Rare:52 | ||||
| chr9:15307204-15307457 | Common:2; Rare:125 | ||||
| chr9:15422605-15422908 | Common:1; Rare:137 | ||||
| chr9:18474003-18474229 | Rare:59 | ||||
| chr9:19049331-19049671 | Common:2; Rare:138 | ||||
| chr9:19049766-19050069 | Common:2; Rare:64 | ||||
| chr9:19102850-19103030 | Common:1; Rare:72 | ||||
| chr9:19127410-19127778 | Common:7; Rare:110 | ||||
| chr9:19380175-19380353 | Common:4; Rare:88 | ||||
| chr9:20684115-20684289 | Common:2; Rare:67 | ||||
| chr9:21802444-21802696 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994605-21994808 | Common:1; Rare:53 | ||||
| chr9:22009239-22009594 | Common:1; Rare:119 | ||||
| chr9:26892737-26892913 | Common:1; Rare:84 | ||||
| chr9:26947107-26947293 | Common:1; Rare:69 |