| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57632647-57632810 | Common:1; Rare:34 | ||||
| chr12:57632882-57632986 | Rare:19 | ||||
| chr12:57716084-57716512 | Common:4; Rare:109 | ||||
| chr12:57744822-57745106 | Common:1; Rare:61 | ||||
| chr12:57745278-57745414 | Common:1; Rare:22 | ||||
| chr12:57751793-57751975 | Rare:33 | ||||
| chr12:57752173-57752708 | Common:1; Rare:135; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:57772058-57772297 | Rare:80 | ||||
| chr12:57772504-57772696 | Common:3; Rare:34 | ||||
| chr12:57846375-57846476 | Rare:32 | ||||
| chr12:57846924-57847221 | Common:2; Rare:109 | ||||
| chr12:57941336-57941699 | Common:5; Rare:105 | ||||
| chr12:57941702-57941813 | Rare:35 | ||||
| chr12:62260068-62260411 | Common:1; Rare:125 | ||||
| chr12:64222259-64222349 | Rare:23 |