| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50188740-50189024 | Rare:73; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50189107-50189307 | Rare:49; Clinvar:2 | ||||
| chr17:50190810-50191133 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:50191948-50192027 | Rare:13 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192797-50193052 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194563-50194829 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr17:50195045-50195361 | Common:1; Rare:96; Clinvar:1; Clinvar (benign):5 | ||||
| chr17:50195427-50195977 | Common:1; Rare:140; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr17:50196152-50196539 | Common:2; Rare:113; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:50198147-50198504 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50199058-50199329 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50199554-50199954 | Common:7; Rare:133; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50201391-50201848 | Common:2; Rare:132; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:50274310-50274547 | Common:2; Rare:64 |