| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16870654-16870807 | Rare:72 | ||||
| chr9:18474003-18474222 | Rare:56 | ||||
| chr9:19049662-19050188 | Common:2; Rare:103 | ||||
| chr9:19102885-19103056 | Common:2; Rare:71 | ||||
| chr9:19127395-19127762 | Common:7; Rare:110 | ||||
| chr9:19380191-19380360 | Common:4; Rare:84 | ||||
| chr9:20684101-20684285 | Common:3; Rare:74 | ||||
| chr9:21994216-21994517 | Rare:112; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr9:21994601-21994700 | Common:1; Rare:23 | ||||
| chr9:21994937-21995108 | Common:1; Rare:28 | ||||
| chr9:26947129-26947304 | Rare:60 | ||||
| chr9:32573037-32573248 | Common:3; Rare:75 | ||||
| chr9:33025092-33025368 | Common:7; Rare:116 | ||||
| chr9:33076597-33076818 | Common:2; Rare:73 | ||||
| chr9:33264706-33265100 | Rare:106 |