| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20621836-20622082 | Common:3; Rare:76 | ||||
| chr9:20622384-20622567 | Rare:75 | ||||
| chr9:20658176-20658356 | Common:4; Rare:66 | ||||
| chr9:20684078-20684292 | Common:3; Rare:85 | ||||
| chr9:20726292-20726481 | Common:1; Rare:38 | ||||
| chr9:21031602-21031790 | Common:1; Rare:61 | ||||
| chr9:21335347-21335561 | Common:3; Rare:90 | ||||
| chr9:21802443-21802700 | Common:3; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:23821631-23821965 | Common:3; Rare:166 | ||||
| chr9:23826069-23826499 | Common:2; Rare:153 | ||||
| chr9:26892426-26892484 | Rare:29 | ||||
| chr9:26892731-26892870 | Rare:68 | ||||
| chr9:26947024-26947273 | Common:1; Rare:95 | ||||
| chr9:26956293-26956466 | Common:2; Rare:61 | ||||
| chr9:27529724-27529899 | Common:5; Rare:53 |