| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970100-6970235 | Rare:46 | ||||
| chr12:6970321-6970452 | Common:1; Rare:47 | ||||
| chr12:6970551-6971032 | Common:5; Rare:157; Clinvar (benign):2 | ||||
| chr12:6971348-6971386 | Rare:9 | ||||
| chr12:6978492-6978794 | Common:3; Rare:69 | ||||
| chr12:6980864-6980983 | Common:1; Rare:26 | ||||
| chr12:6981235-6981505 | Common:2; Rare:36 | ||||
| chr12:6981537-6981907 | Common:2; Rare:86 | ||||
| chr12:7018309-7018879 | Common:3; Rare:170 | ||||
| chr12:7018910-7019061 | Common:3; Rare:33 | ||||
| chr12:7060603-7060749 | Rare:28 | ||||
| chr12:7108210-7108395 | Common:1; Rare:59 | ||||
| chr12:7108418-7108710 | Common:1; Rare:86 | ||||
| chr12:7108904-7109090 | Common:13; Rare:49 | ||||
| chr12:7109158-7109301 | Rare:48 |