| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68277632-68277795 | Common:2; Rare:49 | ||||
| chr15:68817397-68817701 | Common:1; Rare:99 | ||||
| chr15:68820758-68820819 | Rare:22 | ||||
| chr15:69452691-69453020 | Common:5; Rare:137 | ||||
| chr15:70096221-70096362 | Rare:47 | ||||
| chr15:70097856-70098092 | Common:1; Rare:54 | ||||
| chr15:70763409-70763711 | Common:2; Rare:99 | ||||
| chr15:70853949-70854309 | Rare:108 | ||||
| chr15:70892420-70892711 | Common:1; Rare:63 | ||||
| chr15:72118014-72118420 | Common:3; Rare:137 | ||||
| chr15:72231123-72231568 | Common:4; Rare:148 | ||||
| chr15:72375957-72376147 | Common:3; Rare:75; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474174-72474642 | Rare:169 | ||||
| chr15:72686144-72686226 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):2 | ||||
| chr15:72783497-72783613 | Rare:39 |