| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851245-6851499 | Rare:58 | ||||
| chr12:6851887-6852174 | Rare:73 | ||||
| chr12:6867361-6867594 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873334-6873532 | Common:1; Rare:54 | ||||
| chr12:6904740-6904847 | Rare:29 | ||||
| chr12:6951269-6951449 | Rare:50 | ||||
| chr12:6970625-6970976 | Common:4; Rare:113; Clinvar (benign):1 | ||||
| chr12:7108367-7108608 | Common:2; Rare:80 | ||||
| chr12:7189519-7189733 | Rare:73; Clinvar:4 | ||||
| chr12:8914412-8914747 | Common:5; Rare:102 | ||||
| chr12:8949589-8949868 | Common:1; Rare:56 | ||||
| chr12:8949919-8950119 | Common:2; Rare:56 | ||||
| chr12:10613540-10613715 | Common:1; Rare:68 | ||||
| chr12:11170870-11171222 | Common:4; Rare:91 | ||||
| chr12:11171571-11171672 | Common:2; Rare:33 |