| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75667100-75667421 | Common:4; Rare:112 | ||||
| chr17:75765123-75765304 | Common:1; Rare:56; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75779535-75779942 | Common:1; Rare:197 | ||||
| chr17:75784558-75784872 | Common:2; Rare:138 | ||||
| chr17:75784962-75785100 | Common:7; Rare:43 | ||||
| chr17:75785454-75785577 | Common:1; Rare:30 | ||||
| chr17:75840353-75840482 | Common:1; Rare:36; Clinvar (benign):2 | ||||
| chr17:75878552-75878725 | Common:3; Rare:62 | ||||
| chr17:75904809-75905082 | Common:5; Rare:83 | ||||
| chr17:75940989-75941123 | Rare:43 | ||||
| chr17:75941141-75941233 | Common:1; Rare:34 | ||||
| chr17:75979003-75979283 | Rare:80; Clinvar:4 | ||||
| chr17:75979336-75979619 | Common:1; Rare:82; Clinvar (benign):1 | ||||
| chr17:76072321-76072636 | Common:6; Rare:152 | ||||
| chr17:76103673-76103876 | Common:5; Rare:74 |