| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:65169414-65169864 | Common:1; Rare:173; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:66130719-66130918 | Rare:54 | ||||
| chr12:66169892-66170058 | Common:1; Rare:50 | ||||
| chr12:66189083-66189368 | Rare:88; Clinvar:1 | ||||
| chr12:66302327-66302617 | Common:1; Rare:72 | ||||
| chr12:67269567-67269659 | Rare:27 | ||||
| chr12:68332256-68332648 | Common:1; Rare:130 | ||||
| chr12:68610695-68611043 | Common:1; Rare:148 | ||||
| chr12:68686814-68687044 | Common:4; Rare:70 | ||||
| chr12:68746066-68746279 | Common:3; Rare:69 | ||||
| chr12:68807875-68808262 | Common:4; Rare:112 | ||||
| chr12:68808458-68808480 | Rare:7 | ||||
| chr12:68808823-68809061 | Common:1; Rare:49 | ||||
| chr12:68933153-68933343 | Rare:60 | ||||
| chr12:69239480-69239688 | Common:2; Rare:86 |