| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53180896-53181050 | Common:3; Rare:49 | ||||
| chr12:53181295-53181432 | Rare:33 | ||||
| chr12:53232181-53232432 | Common:2; Rare:53 | ||||
| chr12:53252009-53252217 | Common:3; Rare:80 | ||||
| chr12:53321228-53321423 | Common:1; Rare:70; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53452028-53452373 | Rare:87 | ||||
| chr12:53499444-53499652 | Rare:46 | ||||
| chr12:53501213-53501352 | Rare:35 | ||||
| chr12:53625962-53626137 | Common:1; Rare:40 | ||||
| chr12:53626333-53626415 | Common:1; Rare:28 | ||||
| chr12:54281179-54281502 | Common:3; Rare:97 | ||||
| chr12:54403909-54404219 | Rare:74 | ||||
| chr12:54404701-54405057 | Common:1; Rare:87 | ||||
| chr12:54413143-54413327 | Rare:33 | ||||
| chr12:54413643-54413729 | Common:1; Rare:9 |