| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35088047-35088501 | Common:2; Rare:114 | ||||
| chr17:35088822-35089009 | Common:1; Rare:53 | ||||
| chr17:35089094-35089412 | Common:9; Rare:145 | ||||
| chr17:35119536-35120290 | Common:1; Rare:307; Clinvar:23; Clinvar (benign):18; Clinvar (pathogenic):1 | ||||
| chr17:35242917-35243079 | Rare:87 | ||||
| chr17:35578479-35578758 | Common:3; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:35587184-35587543 | Rare:168 | ||||
| chr17:35809283-35809541 | Rare:202 | ||||
| chr17:35981447-35981559 | Rare:31 | ||||
| chr17:36001133-36001371 | Common:2; Rare:39 | ||||
| chr17:36001549-36001888 | Common:1; Rare:47 | ||||
| chr17:36001987-36002305 | Common:10; Rare:110 | ||||
| chr17:36486528-36486751 | Common:5; Rare:150 | ||||
| chr17:36486814-36487214 | Common:1; Rare:206; Clinvar (pathogenic):2 | ||||
| chr17:36534060-36534479 | Common:1; Rare:181 |