| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19379485-19379895 | Common:1; Rare:138 | ||||
| chr9:19380188-19380373 | Common:4; Rare:88 | ||||
| chr9:20684052-20684283 | Common:4; Rare:91 | ||||
| chr9:21031599-21031722 | Common:1; Rare:45 | ||||
| chr9:21802192-21802454 | Common:1; Rare:57 | ||||
| chr9:21994350-21994422 | Rare:27; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:21995307-21995472 | Rare:50 | ||||
| chr9:22008789-22009152 | Common:1; Rare:131 | ||||
| chr9:22009155-22009495 | Common:1; Rare:118 | ||||
| chr9:26892719-26892895 | Common:1; Rare:85 | ||||
| chr9:26947047-26947294 | Common:1; Rare:94 | ||||
| chr9:26947444-26947572 | Common:1; Rare:34 | ||||
| chr9:26956317-26956464 | Common:2; Rare:53 | ||||
| chr9:26976391-26976699 | Rare:60 | ||||
| chr9:27529764-27529899 | Common:4; Rare:43 |