| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73192817-73193067 | Common:15; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232100-73232711 | Common:4; Rare:232 | ||||
| chr17:73310901-73311238 | Common:2; Rare:85 | ||||
| chr17:73311963-73312207 | Rare:63 | ||||
| chr17:74431295-74431423 | Rare:29 | ||||
| chr17:74431745-74431764 | Rare:3 | ||||
| chr17:74432001-74432141 | Common:1; Rare:65 | ||||
| chr17:74466562-74466693 | Rare:37 | ||||
| chr17:74776244-74776543 | Common:4; Rare:97 | ||||
| chr17:75109902-75109969 | Common:1; Rare:17 | ||||
| chr17:75130848-75131084 | Common:2; Rare:80 | ||||
| chr17:75131476-75131815 | Common:4; Rare:141 | ||||
| chr17:75205375-75205749 | Common:1; Rare:121 | ||||
| chr17:75261570-75261945 | Common:4; Rare:122; Clinvar (benign):2 | ||||
| chr17:75271142-75271323 | Common:1; Rare:36 |