| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75516394-75516563 | Rare:50; Clinvar (pathogenic):1 | ||||
| chr17:75525402-75525775 | Common:4; Rare:111 | ||||
| chr17:75543165-75543420 | Common:3; Rare:62 | ||||
| chr17:75624031-75624222 | Common:2; Rare:62 | ||||
| chr17:75633966-75634092 | Rare:25 | ||||
| chr17:75667132-75667466 | Common:5; Rare:113 | ||||
| chr17:75721159-75721541 | Common:3; Rare:117; Clinvar:1 | ||||
| chr17:75765133-75765304 | Common:1; Rare:54; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75784564-75784872 | Common:2; Rare:136 | ||||
| chr17:75844343-75844457 | Rare:27; Clinvar:1 | ||||
| chr17:75844678-75844966 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:75855242-75855699 | Common:1; Rare:131 | ||||
| chr17:75896949-75897095 | Common:2; Rare:64 | ||||
| chr17:75904836-75905218 | Common:5; Rare:109 | ||||
| chr17:75978990-75979298 | Rare:90; Clinvar:4; Clinvar (benign):1 |