| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65278446-65278938 | Common:3; Rare:164; Clinvar (benign):4 | ||||
| chr12:65824947-65825085 | Rare:34 | ||||
| chr12:66130715-66130883 | Rare:52 | ||||
| chr12:66169943-66170115 | Common:1; Rare:49 | ||||
| chr12:67269151-67269443 | Common:2; Rare:86 | ||||
| chr12:67269567-67269725 | Common:1; Rare:61 | ||||
| chr12:67648510-67648776 | Common:3; Rare:67 | ||||
| chr12:68332264-68332615 | Common:1; Rare:115 | ||||
| chr12:68610681-68611028 | Common:1; Rare:153 | ||||
| chr12:68686825-68687034 | Common:4; Rare:63 | ||||
| chr12:68746043-68746283 | Common:3; Rare:75 | ||||
| chr12:68807979-68808258 | Common:3; Rare:92 | ||||
| chr12:68808847-68809034 | Rare:35 | ||||
| chr12:68933160-68933294 | Rare:38 | ||||
| chr12:69239459-69239656 | Common:2; Rare:85 |