| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40342038-40342400 | Common:1; Rare:79 | ||||
| chr17:41524141-41524411 | Common:1; Rare:90 | ||||
| chr17:41524970-41525277 | Common:1; Rare:91; Clinvar:1 | ||||
| chr17:41528072-41528142 | Rare:25 | ||||
| chr17:41688633-41688893 | Common:1; Rare:82 | ||||
| chr17:41689287-41689552 | Common:3; Rare:99 | ||||
| chr17:41786685-41786920 | Common:2; Rare:56 | ||||
| chr17:41812617-41812710 | Common:3; Rare:16 | ||||
| chr17:41812854-41813022 | Rare:47; Clinvar:1 | ||||
| chr17:41930521-41930645 | Rare:31 | ||||
| chr17:41966476-41966837 | Common:3; Rare:107 | ||||
| chr17:42017382-42017510 | Common:1; Rare:55 | ||||
| chr17:42154913-42155168 | Common:3; Rare:66 | ||||
| chr17:42316917-42317215 | Common:3; Rare:54; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:42324976-42325140 | Common:1; Rare:22; Clinvar (benign):3 |