| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120686922-120687210 | Common:2; Rare:100 | ||||
| chr12:120710288-120710502 | Common:3; Rare:71 | ||||
| chr12:120710617-120710721 | Rare:22 | ||||
| chr12:120725733-120725934 | Rare:69; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr12:120903428-120903800 | Common:3; Rare:99 | ||||
| chr12:120904108-120904567 | Common:5; Rare:161 | ||||
| chr12:121016003-121016213 | Common:1; Rare:43 | ||||
| chr12:121016383-121016596 | Common:5; Rare:90 | ||||
| chr12:121038958-121039359 | Common:3; Rare:80 | ||||
| chr12:121132736-121132968 | Rare:47 | ||||
| chr12:121210054-121210330 | Common:3; Rare:113 | ||||
| chr12:121210340-121210502 | Common:1; Rare:32 | ||||
| chr12:121296632-121296989 | Common:2; Rare:106 | ||||
| chr12:121352116-121352218 | Common:1; Rare:40 | ||||
| chr12:121352297-121352872 | Common:10; Rare:177 |