| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47904974-47905151 | Common:1; Rare:55; Clinvar:1 | ||||
| chr12:48105815-48105938 | Rare:28 | ||||
| chr12:48105964-48106137 | Common:1; Rare:51 | ||||
| chr12:48106277-48106385 | Rare:34 | ||||
| chr12:48119190-48119379 | Common:2; Rare:35; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350786-48350953 | Rare:63 | ||||
| chr12:48716628-48716917 | Common:4; Rare:91 | ||||
| chr12:48774721-48775033 | Common:3; Rare:72 | ||||
| chr12:48777479-48777732 | Rare:68 | ||||
| chr12:48814133-48814507 | Common:5; Rare:65 | ||||
| chr12:48814682-48814880 | Rare:37 | ||||
| chr12:48815432-48815617 | Common:1; Rare:43 | ||||
| chr12:48852065-48852315 | Common:2; Rare:80 | ||||
| chr12:48865845-48865969 | Rare:31 | ||||
| chr12:48957367-48957581 | Common:2; Rare:58 |