| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57752243-57752711 | Common:1; Rare:122; Clinvar:1 | ||||
| chr12:57772087-57772280 | Rare:60 | ||||
| chr12:57846376-57846778 | Common:1; Rare:136 | ||||
| chr12:57941360-57941568 | Common:3; Rare:68 | ||||
| chr12:59595930-59596176 | Common:5; Rare:63 | ||||
| chr12:62259978-62260452 | Common:1; Rare:175 | ||||
| chr12:62466648-62466876 | Rare:75 | ||||
| chr12:62467174-62467224 | Rare:16 | ||||
| chr12:63779685-63780192 | Common:4; Rare:203; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:63844391-63844784 | Rare:92 | ||||
| chr12:63844800-63844871 | Common:1; Rare:21 | ||||
| chr12:64222242-64222383 | Rare:48 | ||||
| chr12:64404131-64404659 | Common:7; Rare:182 | ||||
| chr12:64452041-64452174 | Common:1; Rare:48 | ||||
| chr12:64759365-64759585 | Common:1; Rare:67; Clinvar:3 |