| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:58919496-58919612 | Rare:28 | ||||
| chr12:58919960-58920366 | Common:4; Rare:126 | ||||
| chr12:58920469-58920704 | Common:2; Rare:77 | ||||
| chr12:59595856-59596196 | Common:5; Rare:77 | ||||
| chr12:62260041-62260460 | Common:1; Rare:155 | ||||
| chr12:63150922-63150995 | Common:1; Rare:21 | ||||
| chr12:63779764-63780169 | Common:3; Rare:162; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:63844673-63844808 | Rare:36 | ||||
| chr12:64222215-64222378 | Rare:59 | ||||
| chr12:64404256-64404790 | Common:5; Rare:178 | ||||
| chr12:64452022-64452177 | Common:1; Rare:57 | ||||
| chr12:64744828-64745089 | Rare:54 | ||||
| chr12:64759100-64759503 | Common:1; Rare:127; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169441-65169602 | Common:1; Rare:50; Clinvar:1 | ||||
| chr12:65824908-65825099 | Rare:43 |