| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48925490-48925633 | Rare:26 | ||||
| chr12:48957422-48957792 | Common:5; Rare:91 | ||||
| chr12:49018736-49018960 | Common:1; Rare:91 | ||||
| chr12:49131325-49131614 | Common:2; Rare:115 | ||||
| chr12:49188965-49189286 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322970-49323302 | Common:3; Rare:77 | ||||
| chr12:49367214-49367524 | Common:1; Rare:87 | ||||
| chr12:49568110-49568172 | Common:1; Rare:21 | ||||
| chr12:49623250-49623571 | Common:1; Rare:92 | ||||
| chr12:49828407-49828543 | Rare:44 | ||||
| chr12:50025407-50025764 | Common:2; Rare:97 | ||||
| chr12:50112016-50112253 | Common:2; Rare:54 | ||||
| chr12:50167365-50167648 | Common:1; Rare:72 | ||||
| chr12:50400767-50400968 | Rare:61 | ||||
| chr12:50763937-50764503 | Common:4; Rare:159 |