| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43510638-43510964 | Rare:103 | ||||
| chr15:43746282-43746446 | Common:1; Rare:63 | ||||
| chr15:43777114-43777409 | Rare:65 | ||||
| chr15:44288417-44288775 | Common:36; Rare:213 | ||||
| chr15:44536663-44537425 | Common:3; Rare:246 | ||||
| chr15:44711331-44711611 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728869-44729193 | Common:1; Rare:68 | ||||
| chr15:45378520-45378678 | Common:3; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:45587325-45587474 | Rare:43; Clinvar:2 | ||||
| chr15:48331383-48331465 | Rare:27 | ||||
| chr15:48645680-48645929 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr15:48878039-48878394 | Rare:129 | ||||
| chr15:49155523-49155879 | Common:2; Rare:115 | ||||
| chr15:49620752-49621099 | Common:6; Rare:129 | ||||
| chr15:50354923-50354998 | Rare:12 |