| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63054462-63054853 | Common:4; Rare:66 | ||||
| chr15:63060864-63061543 | Common:1; Rare:141; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr15:63062104-63062644 | Common:3; Rare:130; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr15:63063542-63063831 | Common:2; Rare:52 | ||||
| chr15:63121717-63121879 | Rare:50 | ||||
| chr15:63122379-63122585 | Common:3; Rare:66 | ||||
| chr15:63157095-63157295 | Rare:39 | ||||
| chr15:63157374-63157554 | Common:2; Rare:80 | ||||
| chr15:63157978-63158138 | Common:2; Rare:38 | ||||
| chr15:63277286-63277611 | Common:3; Rare:64 | ||||
| chr15:63381764-63381946 | Common:1; Rare:42 | ||||
| chr15:64093776-64094098 | Common:1; Rare:90 | ||||
| chr15:64096080-64096203 | Rare:40 | ||||
| chr15:64162852-64162942 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:64162969-64163281 | Common:4; Rare:103; Clinvar:6; Clinvar (benign):4 |