| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49130701-49131066 | Common:5; Rare:135 | ||||
| chr12:49131298-49131728 | Common:2; Rare:160 | ||||
| chr12:49131766-49132001 | Rare:50 | ||||
| chr12:49188543-49188706 | Common:2; Rare:32 | ||||
| chr12:49188964-49189080 | Rare:40; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264640-49264693 | Rare:12 | ||||
| chr12:49264735-49265229 | Common:6; Rare:177 | ||||
| chr12:49265243-49265328 | Rare:19 | ||||
| chr12:49265533-49265676 | Common:1; Rare:30 | ||||
| chr12:49322855-49323350 | Common:5; Rare:120 | ||||
| chr12:49366539-49366615 | Rare:17 | ||||
| chr12:49366713-49367050 | Common:2; Rare:90 | ||||
| chr12:49367084-49367555 | Common:2; Rare:130 | ||||
| chr12:49567773-49567951 | Rare:49 | ||||
| chr12:49568013-49568339 | Common:2; Rare:81 |