| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48544588-48544651 | Rare:33 | ||||
| chr17:48908295-48908407 | Common:1; Rare:27 | ||||
| chr17:48944765-48944901 | Common:1; Rare:48 | ||||
| chr17:49210591-49210711 | Rare:19 | ||||
| chr17:49677971-49678335 | Rare:92 | ||||
| chr17:49788462-49788759 | Common:1; Rare:100 | ||||
| chr17:50186315-50186928 | Common:2; Rare:173; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188529-50189276 | Rare:188; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192797-50193048 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194129-50194451 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194783 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50195029-50195479 | Common:1; Rare:133; Clinvar:2; Clinvar (benign):6 | ||||
| chr17:50196314-50196603 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50196615-50196938 | Common:2; Rare:69 |