| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34048870-34048953 | Rare:33 | ||||
| chr9:34049186-34049267 | Common:1; Rare:19 | ||||
| chr9:34178937-34179078 | Common:1; Rare:39 | ||||
| chr9:34329198-34329593 | Rare:124 | ||||
| chr9:34376863-34377178 | Common:1; Rare:68 | ||||
| chr9:34458518-34458826 | Common:1; Rare:74 | ||||
| chr9:34612084-34612177 | Rare:28 | ||||
| chr9:35103078-35103157 | Common:1; Rare:41 | ||||
| chr9:35489802-35490113 | Common:1; Rare:99 | ||||
| chr9:35657841-35658429 | Common:11; Rare:468; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35732089-35732344 | Common:1; Rare:75 | ||||
| chr9:35732399-35732671 | Common:2; Rare:64 | ||||
| chr9:35748954-35749338 | Common:2; Rare:136 | ||||
| chr9:35812143-35812281 | Rare:53 | ||||
| chr9:35814983-35815294 | Rare:79 |