| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106303282-106303578 | Common:1; Rare:72 | ||||
| chr12:107093259-107093619 | Common:2; Rare:107 | ||||
| chr12:107318373-107318492 | Common:3; Rare:23 | ||||
| chr12:107320227-107320467 | Rare:43 | ||||
| chr12:107685706-107685939 | Rare:76 | ||||
| chr12:107761102-107761273 | Common:3; Rare:65 | ||||
| chr12:108515058-108515313 | Common:1; Rare:77 | ||||
| chr12:108532228-108532514 | Rare:55 | ||||
| chr12:108535377-108535662 | Common:3; Rare:51 | ||||
| chr12:108538119-108538272 | Common:1; Rare:41 | ||||
| chr12:108562396-108562751 | Common:9; Rare:142; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109098279-109098582 | Rare:129; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:109154552-109154691 | Common:1; Rare:35 | ||||
| chr12:109477260-109477653 | Common:3; Rare:103 | ||||
| chr12:109573435-109573845 | Common:3; Rare:133; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 |