| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62466664-62466831 | Rare:59 | ||||
| chr12:63668459-63668761 | Common:4; Rare:88 | ||||
| chr12:63779760-63779917 | Common:2; Rare:53 | ||||
| chr12:63780087-63780175 | Rare:41; Clinvar (pathogenic):1 | ||||
| chr12:64222242-64222346 | Rare:35 | ||||
| chr12:64759334-64759695 | Common:3; Rare:106; Clinvar:3 | ||||
| chr12:65278884-65278991 | Rare:23 | ||||
| chr12:66130718-66130805 | Rare:29 | ||||
| chr12:66189058-66189342 | Rare:80; Clinvar:1 | ||||
| chr12:68332352-68332636 | Common:1; Rare:82 | ||||
| chr12:68610724-68611041 | Common:1; Rare:130 | ||||
| chr12:68686825-68687050 | Common:4; Rare:68 | ||||
| chr12:68808472-68808485 | Rare:3 | ||||
| chr12:68933148-68933343 | Rare:62 | ||||
| chr12:69470283-69470441 | Common:3; Rare:62 |