| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68277491-68277804 | Common:5; Rare:109 | ||||
| chr15:68817613-68817709 | Common:1; Rare:37 | ||||
| chr15:68820747-68821090 | Rare:105 | ||||
| chr15:68930361-68930553 | Common:2; Rare:64 | ||||
| chr15:69414198-69414356 | Rare:41 | ||||
| chr15:69452694-69453020 | Common:5; Rare:136 | ||||
| chr15:70096183-70096380 | Rare:55 | ||||
| chr15:70892403-70892871 | Common:1; Rare:111 | ||||
| chr15:71115476-71115645 | Common:1; Rare:38 | ||||
| chr15:71547103-71547184 | Common:1; Rare:15 | ||||
| chr15:71547207-71547365 | Rare:39 | ||||
| chr15:72118159-72118434 | Common:2; Rare:90 | ||||
| chr15:72231114-72231455 | Common:3; Rare:108 | ||||
| chr15:72375957-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686149-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 |