| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40345534-40345934 | Common:5; Rare:146 | ||||
| chr17:40363282-40363693 | Common:7; Rare:267 | ||||
| chr17:40416896-40417670 | Common:9; Rare:367 | ||||
| chr17:40417826-40418246 | Rare:651 | ||||
| chr17:40443070-40444032 | Common:15; Rare:851 | ||||
| chr17:40560270-40560660 | Common:4; Rare:166 | ||||
| chr17:40560758-40561158 | Common:7; Rare:114 | ||||
| chr17:40565343-40565743 | Common:3; Rare:148 | ||||
| chr17:40647158-40647594 | Rare:187 | ||||
| chr17:40647730-40648241 | Rare:389 | ||||
| chr17:40648160-40648570 | Common:5; Rare:156 | ||||
| chr17:40648614-40649071 | Common:1; Rare:115 | ||||
| chr17:40818640-40819615 | Common:84; Rare:1971; Clinvar:1; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:40819600-40819753 | Rare:88 | ||||
| chr17:40866840-40867220 | Common:6; Rare:280; Clinvar:6 |