| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3077274-3077447 | Common:5; Rare:76 | ||||
| chr12:3753057-3753222 | Common:1; Rare:43 | ||||
| chr12:3873303-3873527 | Common:4; Rare:48 | ||||
| chr12:4273905-4274052 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr12:4274093-4274235 | Rare:32 | ||||
| chr12:4275444-4275703 | Common:3; Rare:45 | ||||
| chr12:4320942-4321260 | Common:5; Rare:121 | ||||
| chr12:4538431-4538909 | Common:2; Rare:106 | ||||
| chr12:4649001-4649185 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr12:6124528-6124762 | Rare:32; Clinvar:1 | ||||
| chr12:6124893-6124953 | Rare:18 | ||||
| chr12:6200005-6200559 | Common:4; Rare:166 | ||||
| chr12:6200662-6200701 | Rare:9 | ||||
| chr12:6225275-6225531 | Rare:76 | ||||
| chr12:6363912-6363925 | Rare:3 |