| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64093759-64094153 | Common:2; Rare:115 | ||||
| chr15:64096080-64096169 | Rare:27 | ||||
| chr15:64162851-64163077 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):3 | ||||
| chr15:64387615-64387965 | Common:3; Rare:126 | ||||
| chr15:64825612-64825762 | Common:1; Rare:30 | ||||
| chr15:64980948-64981278 | Common:4; Rare:75; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr15:64989660-64990092 | Common:4; Rare:141; Clinvar:3; Clinvar (benign):1 | ||||
| chr15:65119904-65120123 | Common:1; Rare:58 | ||||
| chr15:65133545-65133887 | Common:1; Rare:112 | ||||
| chr15:65286838-65287088 | Rare:75 | ||||
| chr15:65517266-65517315 | Common:1; Rare:19 | ||||
| chr15:65517472-65517730 | Common:2; Rare:89 | ||||
| chr15:65611066-65611413 | Common:3; Rare:118 | ||||
| chr15:65792055-65792454 | Common:3; Rare:110 | ||||
| chr15:65869412-65869622 | Rare:80 |