| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48350777-48350963 | Rare:66 | ||||
| chr12:48716649-48717008 | Common:4; Rare:107 | ||||
| chr12:48814703-48814854 | Rare:29 | ||||
| chr12:48815296-48815595 | Common:1; Rare:70 | ||||
| chr12:48852127-48852348 | Common:2; Rare:64 | ||||
| chr12:48925475-48925796 | Common:2; Rare:67 | ||||
| chr12:49018736-49018937 | Common:1; Rare:84 | ||||
| chr12:49110661-49110783 | Rare:24 | ||||
| chr12:49129717-49129864 | Common:4; Rare:43 | ||||
| chr12:49130274-49130516 | Common:1; Rare:95 | ||||
| chr12:49130785-49130919 | Common:3; Rare:53 | ||||
| chr12:49131296-49131617 | Common:2; Rare:125 | ||||
| chr12:49188455-49188638 | Common:2; Rare:25 | ||||
| chr12:49188981-49189136 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49189183-49189277 | Rare:21 |