| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127424253-127424441 | Common:1; Rare:62 | ||||
| chr9:127449347-127449707 | Common:2; Rare:94 | ||||
| chr9:127451272-127451565 | Common:3; Rare:121; Clinvar (benign):1 | ||||
| chr9:127579011-127579339 | Common:4; Rare:64 | ||||
| chr9:127612047-127612314 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:127877662-127877798 | Rare:26 | ||||
| chr9:128098317-128098537 | Common:1; Rare:44 | ||||
| chr9:128149280-128149457 | Rare:33 | ||||
| chr9:128160018-128160405 | Common:2; Rare:91 | ||||
| chr9:128275903-128276312 | Common:5; Rare:181 | ||||
| chr9:128322397-128322621 | Common:1; Rare:68 | ||||
| chr9:128322751-128322896 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128340433-128340746 | Common:2; Rare:95 | ||||
| chr9:128371159-128371389 | Common:1; Rare:79 | ||||
| chr9:128552408-128552597 | Rare:73; Clinvar:1 |