| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68277655-68277787 | Common:2; Rare:39 | ||||
| chr15:68817605-68817699 | Common:1; Rare:34 | ||||
| chr15:68820733-68821090 | Rare:106 | ||||
| chr15:69160342-69160662 | Common:4; Rare:98 | ||||
| chr15:69298786-69298967 | Common:3; Rare:40 | ||||
| chr15:69414208-69414372 | Rare:46 | ||||
| chr15:69452684-69453020 | Common:5; Rare:140 | ||||
| chr15:70097856-70098092 | Common:1; Rare:54 | ||||
| chr15:70763333-70763840 | Common:2; Rare:164 | ||||
| chr15:70854034-70854295 | Rare:78 | ||||
| chr15:70892403-70892823 | Common:1; Rare:92 | ||||
| chr15:72118167-72118434 | Common:2; Rare:88 | ||||
| chr15:72231102-72231520 | Common:3; Rare:132 | ||||
| chr15:72375957-72376137 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474178-72474351 | Rare:63 |