| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6914385-6914612 | Rare:57 | ||||
| chr12:6943926-6944124 | Common:8; Rare:203; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:6970602-6970983 | Common:4; Rare:123; Clinvar (benign):1 | ||||
| chr12:7018468-7018591 | Common:1; Rare:32 | ||||
| chr12:7108481-7108608 | Common:1; Rare:40 | ||||
| chr12:7189525-7189726 | Rare:69; Clinvar:4 | ||||
| chr12:8914374-8914714 | Common:6; Rare:99 | ||||
| chr12:8949440-8949495 | Rare:8 | ||||
| chr12:8949582-8950112 | Common:4; Rare:125 | ||||
| chr12:10212237-10212511 | Rare:77 | ||||
| chr12:10613473-10613725 | Common:1; Rare:99 | ||||
| chr12:11171147-11171237 | Rare:33 | ||||
| chr12:11171551-11171732 | Common:2; Rare:61 | ||||
| chr12:11649752-11650013 | Common:1; Rare:79 | ||||
| chr12:12356981-12357182 | Common:4; Rare:105 |