| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35748910-35749076 | Common:2; Rare:33 | ||||
| chr9:35814989-35815323 | Common:1; Rare:85 | ||||
| chr9:36258409-36258576 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37800707-37800822 | Rare:34 | ||||
| chr9:38392593-38392723 | Common:1; Rare:35 | ||||
| chr9:70258853-70259060 | Common:2; Rare:96 | ||||
| chr9:71911163-71911523 | Common:3; Rare:108 | ||||
| chr9:75088098-75088586 | Common:4; Rare:166 | ||||
| chr9:78236017-78236110 | Rare:31 | ||||
| chr9:81689486-81689829 | Common:10; Rare:139 | ||||
| chr9:83707901-83708292 | Common:3; Rare:125 | ||||
| chr9:83980161-83980356 | Rare:68 | ||||
| chr9:83980552-83980783 | Common:3; Rare:97 | ||||
| chr9:86282051-86282204 | Common:4; Rare:52 | ||||
| chr9:87974521-87974658 | Common:1; Rare:29 |