| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63844801-63844879 | Common:1; Rare:23 | ||||
| chr12:64222200-64222400 | Common:1; Rare:73 | ||||
| chr12:64390450-64390730 | Rare:94 | ||||
| chr12:64404221-64404598 | Common:4; Rare:144 | ||||
| chr12:64405009-64405074 | Rare:10 | ||||
| chr12:64451997-64452522 | Common:2; Rare:169 | ||||
| chr12:64759330-64759518 | Common:1; Rare:63; Clinvar:3 | ||||
| chr12:64780701-64780777 | Rare:16 | ||||
| chr12:65169471-65169611 | Common:1; Rare:50; Clinvar:2 | ||||
| chr12:65169636-65170055 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):3 | ||||
| chr12:65278627-65278732 | Rare:28 | ||||
| chr12:66130645-66130864 | Common:1; Rare:80 | ||||
| chr12:66169943-66170336 | Common:2; Rare:95 | ||||
| chr12:66189074-66189302 | Rare:57 | ||||
| chr12:66302262-66302596 | Common:1; Rare:78 |