| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:32539238-32539872 | Common:18; Rare:188 | ||||
| chr1:32539883-32539919 | Rare:4 | ||||
| chr1:32650270-32650355 | Rare:14 | ||||
| chr1:32650406-32650719 | Common:1; Rare:121 | ||||
| chr1:32650878-32651356 | Common:2; Rare:176 | ||||
| chr1:32651383-32651571 | Common:4; Rare:48 | ||||
| chr1:32651576-32651643 | Common:2; Rare:24 | ||||
| chr1:32753844-32754020 | Common:2; Rare:61 | ||||
| chr1:32816907-32817003 | Rare:19 | ||||
| chr1:32817073-32817142 | Rare:11 | ||||
| chr1:32817242-32817752 | Common:1; Rare:138; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:32817766-32817850 | Rare:14; Clinvar (benign):1 | ||||
| chr1:32817854-32818137 | Common:4; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:32818142-32818459 | Rare:88 | ||||
| chr1:32893823-32893996 | Rare:47; Clinvar (pathogenic):1 |