| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64611523-64611715 | Common:1; Rare:38 | ||||
| chr12:64623425-64623576 | Rare:18 | ||||
| chr12:64625347-64625745 | Common:3; Rare:133 | ||||
| chr12:64625756-64625946 | Common:1; Rare:44 | ||||
| chr12:64671766-64671957 | Common:3; Rare:28 | ||||
| chr12:64672930-64673270 | Common:4; Rare:74 | ||||
| chr12:64673610-64674140 | Common:1; Rare:101 | ||||
| chr12:64820647-64821365 | Common:4; Rare:131 | ||||
| chr12:64889885-64890206 | Rare:84 | ||||
| chr12:65170390-65171125 | Common:3; Rare:544; Clinvar:21; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:65187197-65188129 | Common:2; Rare:306 | ||||
| chr12:65607490-65607870 | Common:2; Rare:66 | ||||
| chr12:65868395-65868533 | Rare:27 | ||||
| chr12:66229662-66230423 | Common:3; Rare:273 | ||||
| chr12:66235221-66235621 | Common:6; Rare:175 |