| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63780069-63780192 | Rare:59; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:63844635-63844759 | Rare:27 | ||||
| chr12:64222197-64222380 | Rare:68 | ||||
| chr12:64404189-64404754 | Common:5; Rare:196 | ||||
| chr12:64404762-64404804 | Rare:8 | ||||
| chr12:64404957-64405117 | Rare:34 | ||||
| chr12:64452041-64452360 | Common:1; Rare:107 | ||||
| chr12:64610559-64610627 | Common:1; Rare:25 | ||||
| chr12:64759353-64759667 | Common:3; Rare:92; Clinvar:3 | ||||
| chr12:65169452-65169588 | Common:1; Rare:46 | ||||
| chr12:65824924-65825099 | Rare:38 | ||||
| chr12:66130694-66130878 | Rare:61 | ||||
| chr12:66169574-66169712 | Common:1; Rare:39 | ||||
| chr12:66169904-66170088 | Common:1; Rare:55 | ||||
| chr12:66302300-66302617 | Common:1; Rare:78 |