| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34048876-34049012 | Common:1; Rare:54 | ||||
| chr9:34329195-34329619 | Common:1; Rare:133 | ||||
| chr9:35103084-35103407 | Common:1; Rare:98 | ||||
| chr9:35657972-35658322 | Common:5; Rare:272; Clinvar:20; Clinvar (benign):10; Clinvar (pathogenic):34 | ||||
| chr9:35689885-35690099 | Common:3; Rare:66; Clinvar:3 | ||||
| chr9:35732089-35732361 | Common:1; Rare:85 | ||||
| chr9:35749004-35749357 | Common:2; Rare:134 | ||||
| chr9:36190734-36190973 | Common:1; Rare:82 | ||||
| chr9:37422595-37422730 | Common:2; Rare:70 | ||||
| chr9:37485737-37486006 | Common:1; Rare:96 | ||||
| chr9:69759930-69760113 | Common:2; Rare:85 | ||||
| chr9:70258845-70259077 | Common:3; Rare:108 | ||||
| chr9:78296869-78297206 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr9:83707874-83708294 | Common:3; Rare:136 | ||||
| chr9:83979612-83979743 | Rare:40 |