| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:21031599-21031691 | Common:1; Rare:36 | ||||
| chr9:21802199-21802534 | Common:3; Rare:79 | ||||
| chr9:21802593-21802687 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:26892738-26892887 | Common:1; Rare:75 | ||||
| chr9:26947024-26947290 | Common:1; Rare:101 | ||||
| chr9:26956246-26956459 | Common:2; Rare:79 | ||||
| chr9:27573430-27573514 | Common:2; Rare:45 | ||||
| chr9:32384503-32384732 | Common:1; Rare:86 | ||||
| chr9:32573064-32573302 | Common:4; Rare:85 | ||||
| chr9:33001560-33001813 | Common:3; Rare:114; Clinvar (benign):3 | ||||
| chr9:33025065-33025312 | Common:6; Rare:104 | ||||
| chr9:33076605-33076812 | Common:2; Rare:73 | ||||
| chr9:33166843-33166956 | Rare:41 | ||||
| chr9:33290352-33290578 | Common:2; Rare:83 | ||||
| chr9:33473845-33474151 | Common:4; Rare:94 |