| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48839850-48840074 | Rare:56 | ||||
| chr12:48852102-48852403 | Common:2; Rare:82 | ||||
| chr12:48925481-48925646 | Common:1; Rare:32 | ||||
| chr12:49018736-49018927 | Common:1; Rare:78 | ||||
| chr12:49131274-49131617 | Common:2; Rare:138 | ||||
| chr12:49188482-49188621 | Common:2; Rare:18 | ||||
| chr12:49188977-49189222 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264757-49265087 | Common:4; Rare:116 | ||||
| chr12:49294912-49295148 | Common:3; Rare:46 | ||||
| chr12:49568104-49568223 | Common:2; Rare:38 | ||||
| chr12:49707254-49707739 | Common:2; Rare:135 | ||||
| chr12:49828381-49828595 | Common:1; Rare:79 | ||||
| chr12:50167298-50167694 | Common:3; Rare:107 | ||||
| chr12:50283470-50283665 | Common:2; Rare:63 | ||||
| chr12:50400719-50400979 | Rare:80 |