| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6946335-6946644 | Common:1; Rare:82 | ||||
| chr12:6970195-6970373 | Rare:65 | ||||
| chr12:6970415-6970976 | Common:4; Rare:177; Clinvar (benign):1 | ||||
| chr12:7018331-7018584 | Common:2; Rare:76 | ||||
| chr12:7018773-7018800 | Rare:7 | ||||
| chr12:7060390-7060867 | Rare:96 | ||||
| chr12:7108353-7108570 | Common:2; Rare:76 | ||||
| chr12:7128868-7129224 | Common:2; Rare:49 | ||||
| chr12:7130256-7130423 | Common:4; Rare:45 | ||||
| chr12:7189620-7189735 | Rare:47; Clinvar:4 | ||||
| chr12:7502449-7502779 | Common:2; Rare:76 | ||||
| chr12:8032591-8032811 | Rare:74 | ||||
| chr12:8033507-8033577 | Rare:14 | ||||
| chr12:8066311-8066571 | Rare:36 | ||||
| chr12:8227599-8227684 | Rare:25 |