| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62933560-62933768 | Common:3; Rare:40 | ||||
| chr12:62934588-62934883 | Common:1; Rare:102 | ||||
| chr12:62935044-62935470 | Common:2; Rare:104 | ||||
| chr12:63779663-63779955 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chr12:63780063-63780234 | Rare:80; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:63780293-63780417 | Rare:22 | ||||
| chr12:63843632-63843922 | Common:3; Rare:83 | ||||
| chr12:63843931-63844274 | Common:3; Rare:67 | ||||
| chr12:63844461-63844602 | Rare:29 | ||||
| chr12:63844967-63845072 | Common:1; Rare:20 | ||||
| chr12:63845110-63845320 | Rare:38 | ||||
| chr12:64221776-64222098 | Rare:68 | ||||
| chr12:64222202-64222413 | Common:1; Rare:77 | ||||
| chr12:64222446-64222646 | Common:1; Rare:30 | ||||
| chr12:64293228-64293410 | Common:4; Rare:46 |