| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64024792-64024933 | Common:1; Rare:29 | ||||
| chr15:64246760-64247160 | Common:2; Rare:69 | ||||
| chr15:64461394-64461794 | Common:4; Rare:119 | ||||
| chr15:64536090-64536620 | Common:3; Rare:94 | ||||
| chr15:64835722-64836009 | Common:3; Rare:70 | ||||
| chr15:65033132-65033388 | Common:2; Rare:48 | ||||
| chr15:65033679-65034079 | Common:3; Rare:91 | ||||
| chr15:65044313-65044426 | Common:1; Rare:17 | ||||
| chr15:65049397-65049589 | Common:4; Rare:48 | ||||
| chr15:65057602-65057777 | Rare:34 | ||||
| chr15:65077850-65078490 | Common:4; Rare:215; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr15:65132965-65133091 | Rare:57 | ||||
| chr15:65189190-65189430 | Common:1; Rare:47 | ||||
| chr15:65275707-65276107 | Common:5; Rare:144 | ||||
| chr15:65295797-65296284 | Common:6; Rare:328 |