| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68511758-68512039 | Rare:76 | ||||
| chr17:68512302-68512574 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:69327045-69327334 | Common:2; Rare:94 | ||||
| chr17:70169338-70169554 | Common:1; Rare:57 | ||||
| chr17:72120793-72121034 | Rare:63 | ||||
| chr17:73192817-73193096 | Common:15; Rare:117; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:73232230-73232694 | Common:3; Rare:165 | ||||
| chr17:73311962-73312349 | Rare:101 | ||||
| chr17:74213319-74213578 | Common:4; Rare:56 | ||||
| chr17:74748421-74748684 | Common:4; Rare:100 | ||||
| chr17:74748926-74749236 | Common:3; Rare:119; Clinvar:2 | ||||
| chr17:74776288-74776520 | Common:4; Rare:72 | ||||
| chr17:75012602-75012689 | Rare:21 | ||||
| chr17:75032433-75032605 | Rare:22 | ||||
| chr17:75042209-75042362 | Rare:36 |