| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970566-6970971 | Common:4; Rare:128; Clinvar (benign):1 | ||||
| chr12:7108530-7108703 | Common:1; Rare:38 | ||||
| chr12:8032617-8032785 | Rare:60 | ||||
| chr12:11171597-11171705 | Common:1; Rare:35 | ||||
| chr12:12357020-12357138 | Common:1; Rare:62 | ||||
| chr12:12611670-12611921 | Common:2; Rare:75 | ||||
| chr12:14365490-14365682 | Common:1; Rare:57 | ||||
| chr12:14567893-14567945 | Rare:8 | ||||
| chr12:14803437-14803687 | Common:1; Rare:64 | ||||
| chr12:15882325-15882666 | Common:1; Rare:96 | ||||
| chr12:21501571-21501841 | Common:1; Rare:65 | ||||
| chr12:25195151-25195328 | Common:1; Rare:53 | ||||
| chr12:26938287-26938527 | Common:3; Rare:89 | ||||
| chr12:27710748-27710885 | Common:2; Rare:64 | ||||
| chr12:28190355-28190476 | Common:1; Rare:36 |