| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:10019775-10020095 | Common:1; Rare:88 | ||||
| chr17:10036745-10037074 | Common:4; Rare:51 | ||||
| chr17:10059752-10059916 | Rare:33 | ||||
| chr17:10697417-10697654 | Common:3; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:10729531-10729806 | Common:3; Rare:98 | ||||
| chr17:10729974-10730080 | Common:3; Rare:24 | ||||
| chr17:12665832-12666185 | Common:2; Rare:79 | ||||
| chr17:14069361-14069618 | Common:2; Rare:95; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:14300796-14301116 | Common:3; Rare:84 | ||||
| chr17:15262449-15262668 | Rare:50 | ||||
| chr17:15699506-15699785 | Common:3; Rare:75 | ||||
| chr17:15999600-15999824 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:16039597-16039860 | Common:2; Rare:65 | ||||
| chr17:16215532-16215606 | Rare:29 | ||||
| chr17:16569149-16569330 | Common:1; Rare:62 |