| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851238-6851492 | Rare:60 | ||||
| chr12:6851902-6852179 | Rare:73 | ||||
| chr12:6867371-6867615 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6904676-6904852 | Rare:41 | ||||
| chr12:6914371-6914627 | Rare:62 | ||||
| chr12:6970607-6970961 | Common:3; Rare:109 | ||||
| chr12:7018468-7018580 | Common:1; Rare:30 | ||||
| chr12:7189540-7189726 | Rare:68; Clinvar:4 | ||||
| chr12:8032583-8032770 | Common:3; Rare:66 | ||||
| chr12:8033477-8033751 | Rare:70 | ||||
| chr12:8662628-8662859 | Common:4; Rare:49 | ||||
| chr12:8914389-8914764 | Common:6; Rare:114 | ||||
| chr12:9869323-9869603 | Common:3; Rare:43 | ||||
| chr12:10212356-10212526 | Rare:48 | ||||
| chr12:10213487-10213646 | Common:1; Rare:34 |