| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35079996-35080153 | Common:3; Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:35103078-35103292 | Common:1; Rare:73 | ||||
| chr9:35161828-35161981 | Common:3; Rare:48 | ||||
| chr9:35619529-35619619 | Rare:20 | ||||
| chr9:35650611-35650782 | Rare:55 | ||||
| chr9:35650883-35651022 | Rare:38 | ||||
| chr9:35657874-35658342 | Common:7; Rare:398; Clinvar:37; Clinvar (benign):14; Clinvar (pathogenic):37 | ||||
| chr9:35665172-35665345 | Common:2; Rare:65 | ||||
| chr9:35732083-35732334 | Common:2; Rare:70 | ||||
| chr9:35732373-35732636 | Common:2; Rare:66 | ||||
| chr9:35748992-35749342 | Common:2; Rare:131 | ||||
| chr9:35812236-35812297 | Rare:23 | ||||
| chr9:35814972-35815275 | Rare:75 | ||||
| chr9:36190703-36190964 | Common:1; Rare:91 | ||||
| chr9:36258404-36258625 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 |