| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32399632-32399892 | Common:2; Rare:77 | ||||
| chr12:32679157-32679366 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755371-32755624 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:32755746-32756021 | Rare:104; Clinvar (benign):1 | ||||
| chr12:32896755-32896846 | Rare:35; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:34022284-34022526 | Common:2; Rare:65 | ||||
| chr12:38905449-38905722 | Common:4; Rare:76 | ||||
| chr12:39332398-39332706 | Common:2; Rare:88; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:39443692-39443859 | Rare:37 | ||||
| chr12:40224374-40224763 | Common:1; Rare:99 | ||||
| chr12:40224890-40225071 | Common:3; Rare:48; Clinvar (benign):1 | ||||
| chr12:40225436-40225626 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:40692412-40692586 | Common:1; Rare:46 | ||||
| chr12:42144429-42144596 | Common:2; Rare:45 | ||||
| chr12:42237417-42237779 | Rare:109 |