| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48903843-48904144 | Common:8; Rare:67 | ||||
| chr12:48924559-48924775 | Common:2; Rare:64 | ||||
| chr12:48925298-48925327 | Rare:9 | ||||
| chr12:48925344-48925428 | Rare:32 | ||||
| chr12:48957367-48957657 | Common:4; Rare:79 | ||||
| chr12:49018735-49018947 | Common:1; Rare:88 | ||||
| chr12:49110647-49110787 | Rare:29 | ||||
| chr12:49110840-49111167 | Rare:72 | ||||
| chr12:49131296-49131569 | Rare:112 | ||||
| chr12:49188487-49188660 | Common:2; Rare:24 | ||||
| chr12:49188979-49189298 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265092 | Common:4; Rare:113 | ||||
| chr12:49322952-49323311 | Common:3; Rare:92 | ||||
| chr12:49367234-49367548 | Common:1; Rare:84 | ||||
| chr12:49568104-49568223 | Common:2; Rare:38 |