| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21418390-21418796 | Common:10; Rare:233 | ||||
| chr12:21418980-21420056 | Common:49; Rare:963 | ||||
| chr12:21437360-21438439 | Common:50; Rare:960 | ||||
| chr12:21501501-21501924 | Common:21; Rare:620 | ||||
| chr12:21657016-21657610 | Common:3; Rare:208 | ||||
| chr12:21657699-21658102 | Common:17; Rare:385; Clinvar:8; Clinvar (benign):4 | ||||
| chr12:21774040-21774687 | Common:6; Rare:314; Clinvar (benign):2 | ||||
| chr12:21774640-21775782 | Common:3; Rare:747 | ||||
| chr12:21941329-21941922 | Common:3; Rare:135 | ||||
| chr12:22045960-22046772 | Common:10; Rare:457 | ||||
| chr12:22046690-22047260 | Common:4; Rare:296 | ||||
| chr12:22543525-22543925 | Common:4; Rare:174 | ||||
| chr12:22544040-22544786 | Common:13; Rare:838 | ||||
| chr12:22624824-22625269 | Common:4; Rare:684 | ||||
| chr12:22625266-22625666 | Common:4; Rare:204 |