| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19408785-19409028 | Common:3; Rare:94 | ||||
| chr9:20684040-20684313 | Common:4; Rare:106 | ||||
| chr9:21031583-21031661 | Common:1; Rare:40 | ||||
| chr9:21335046-21335133 | Rare:22 | ||||
| chr9:21859013-21859311 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr9:21974811-21974890 | Common:1; Rare:35; Clinvar:10; Clinvar (benign):9 | ||||
| chr9:21975022-21975295 | Common:1; Rare:69 | ||||
| chr9:21994173-21994842 | Common:2; Rare:209; Clinvar:16; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr9:21994923-21995074 | Common:1; Rare:24 | ||||
| chr9:25678379-25678539 | Rare:47 | ||||
| chr9:26892312-26892524 | Rare:103 | ||||
| chr9:26892657-26892891 | Common:1; Rare:112 | ||||
| chr9:26946901-26947308 | Common:1; Rare:153; Clinvar (pathogenic):1 | ||||
| chr9:26947403-26947558 | Common:1; Rare:54 | ||||
| chr9:26956283-26956497 | Common:2; Rare:82 |