| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684037-20684293 | Common:4; Rare:100 | ||||
| chr9:21031577-21031690 | Common:1; Rare:50 | ||||
| chr9:21994231-21994828 | Common:2; Rare:186; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr9:26892319-26892550 | Rare:113 | ||||
| chr9:26946905-26947293 | Common:1; Rare:150; Clinvar (pathogenic):1 | ||||
| chr9:26947409-26947557 | Common:1; Rare:50 | ||||
| chr9:27109463-27109542 | Rare:15; Clinvar (benign):1 | ||||
| chr9:33025098-33025379 | Common:6; Rare:116 | ||||
| chr9:33076610-33076756 | Common:2; Rare:60 | ||||
| chr9:33264599-33265108 | Common:1; Rare:149 | ||||
| chr9:33473843-33474172 | Common:4; Rare:100 | ||||
| chr9:34048833-34049056 | Common:2; Rare:93 | ||||
| chr9:34049181-34049267 | Common:1; Rare:20 | ||||
| chr9:34126361-34126608 | Rare:91 | ||||
| chr9:34329186-34329611 | Common:1; Rare:135 |