| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64222233-64222391 | Rare:56 | ||||
| chr12:64404239-64404754 | Common:5; Rare:178 | ||||
| chr12:64452019-64452344 | Common:1; Rare:111 | ||||
| chr12:64610559-64610677 | Common:1; Rare:35 | ||||
| chr12:64759084-64759503 | Common:1; Rare:131; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169452-65169588 | Common:1; Rare:46 | ||||
| chr12:66130686-66130889 | Rare:65 | ||||
| chr12:66169854-66170115 | Common:1; Rare:73 | ||||
| chr12:66189125-66189342 | Rare:66; Clinvar:1 | ||||
| chr12:67269149-67269390 | Common:1; Rare:69 | ||||
| chr12:67269519-67269708 | Common:1; Rare:71 | ||||
| chr12:68332265-68332646 | Common:1; Rare:127 | ||||
| chr12:68610724-68611050 | Common:1; Rare:130 | ||||
| chr12:68686805-68687044 | Common:5; Rare:76 | ||||
| chr12:68746066-68746283 | Common:3; Rare:69 |