| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68498072-68498327 | Common:3; Rare:39 | ||||
| chr17:68774636-68774952 | Common:4; Rare:48 | ||||
| chr17:69093531-69093668 | Rare:25 | ||||
| chr17:69503858-69503906 | Rare:8 | ||||
| chr17:69516908-69517267 | Common:1; Rare:59 | ||||
| chr17:69607235-69607431 | Rare:35 | ||||
| chr17:72006166-72006231 | Common:2; Rare:9 | ||||
| chr17:72029955-72030326 | Common:3; Rare:78 | ||||
| chr17:72030393-72030601 | Common:3; Rare:46 | ||||
| chr17:72034083-72034234 | Rare:25 | ||||
| chr17:72122078-72122231 | Rare:22 | ||||
| chr17:72122804-72122839 | Rare:11; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:72317902-72318026 | Rare:23 | ||||
| chr17:72419917-72420236 | Common:2; Rare:57 | ||||
| chr17:72421239-72421614 | Common:1; Rare:62 |