| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105997-48106063 | Rare:15 | ||||
| chr12:48106141-48106158 | Common:1; Rare:4 | ||||
| chr12:48716681-48717008 | Common:4; Rare:97 | ||||
| chr12:49018739-49018877 | Rare:60 | ||||
| chr12:49131296-49131617 | Common:2; Rare:125 | ||||
| chr12:49188482-49188597 | Common:1; Rare:16 | ||||
| chr12:49188975-49189298 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264758-49265096 | Common:4; Rare:120 | ||||
| chr12:49322980-49323323 | Common:3; Rare:79 | ||||
| chr12:49367234-49367539 | Common:1; Rare:83 | ||||
| chr12:49568104-49568192 | Common:2; Rare:29 | ||||
| chr12:49828411-49828575 | Rare:52 | ||||
| chr12:50085287-50085355 | Rare:16 | ||||
| chr12:50167293-50167645 | Common:3; Rare:100 | ||||
| chr12:50283508-50283652 | Common:1; Rare:43 |