| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64975440-64975727 | Common:2; Rare:100 | ||||
| chr17:65100712-65100896 | Rare:55 | ||||
| chr17:68101481-68101566 | Common:3; Rare:44 | ||||
| chr17:68205334-68205494 | Common:6; Rare:45 | ||||
| chr17:75750767-75751032 | Rare:84; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr17:76557631-76557854 | Common:1; Rare:78 | ||||
| chr17:77390229-77390295 | Rare:15 | ||||
| chr17:77452054-77452278 | Rare:41 | ||||
| chr17:78179519-78179677 | Rare:37 | ||||
| chr17:78416936-78417245 | Common:2; Rare:69 | ||||
| chr17:80071434-80071704 | Common:2; Rare:52 | ||||
| chr17:80773659-80773897 | Common:2; Rare:48 | ||||
| chr17:81932066-81932173 | Common:1; Rare:26 | ||||
| chr18:3603478-3603739 | Common:1; Rare:41 | ||||
| chr18:5238005-5238174 | Common:1; Rare:59 |