| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62305889-62305919 | Rare:4 | ||||
| chr12:62466676-62466844 | Rare:58 | ||||
| chr12:62467017-62467158 | Rare:22 | ||||
| chr12:62578171-62578213 | Rare:7 | ||||
| chr12:63779658-63779915 | Common:3; Rare:88 | ||||
| chr12:63843685-63844240 | Common:5; Rare:134 | ||||
| chr12:63844295-63844635 | Common:2; Rare:69 | ||||
| chr12:63844664-63844862 | Common:1; Rare:58 | ||||
| chr12:63844928-63845137 | Common:2; Rare:38 | ||||
| chr12:64222242-64222355 | Rare:39 | ||||
| chr12:64404456-64404801 | Common:3; Rare:113 | ||||
| chr12:64409793-64410007 | Common:1; Rare:39 | ||||
| chr12:64451761-64452174 | Common:2; Rare:133 | ||||
| chr12:64759097-64759539 | Common:1; Rare:140; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65278566-65278821 | Common:2; Rare:92; Clinvar (benign):2 |