| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63550517-63550675 | Common:1; Rare:32 | ||||
| chr17:63600763-63600922 | Rare:43; Clinvar:2 | ||||
| chr17:63621901-63621976 | Rare:29 | ||||
| chr17:63700080-63700341 | Common:1; Rare:67 | ||||
| chr17:63741759-63741993 | Common:3; Rare:103 | ||||
| chr17:63773466-63773859 | Common:2; Rare:127 | ||||
| chr17:63774057-63774329 | Common:10; Rare:118 | ||||
| chr17:63826892-63826992 | Common:1; Rare:24 | ||||
| chr17:63826997-63827503 | Common:5; Rare:151 | ||||
| chr17:64263214-64263425 | Common:2; Rare:85 | ||||
| chr17:64496997-64497163 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:64506146-64506689 | Common:7; Rare:216 | ||||
| chr17:64506734-64506878 | Rare:64 | ||||
| chr17:64662305-64662426 | Common:1; Rare:56 | ||||
| chr17:64919459-64919620 | Common:5; Rare:29 |