| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6663093-6663403 | Common:2; Rare:88 | ||||
| chr12:6689350-6689755 | Common:3; Rare:107 | ||||
| chr12:6723844-6724296 | Common:1; Rare:97 | ||||
| chr12:6851262-6851385 | Rare:24 | ||||
| chr12:6851893-6852174 | Rare:72 | ||||
| chr12:6867377-6867555 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6869229-6869282 | Rare:13 | ||||
| chr12:6873291-6873659 | Common:3; Rare:108 | ||||
| chr12:6904627-6904847 | Common:1; Rare:49 | ||||
| chr12:6970427-6970435 | Rare:4 | ||||
| chr12:6970560-6970961 | Common:3; Rare:124 | ||||
| chr12:7108486-7108608 | Common:1; Rare:37 | ||||
| chr12:7189549-7189726 | Rare:65; Clinvar:4 | ||||
| chr12:8227599-8227691 | Rare:26 | ||||
| chr12:8540814-8541004 | Common:3; Rare:42 |