| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6943926-6944300 | Common:10; Rare:315; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6970640-6970979 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr12:7018431-7018584 | Common:1; Rare:46 | ||||
| chr12:7130250-7130423 | Common:5; Rare:46 | ||||
| chr12:8032568-8032759 | Common:4; Rare:66 | ||||
| chr12:8066331-8066550 | Rare:31 | ||||
| chr12:8227579-8227692 | Rare:29 | ||||
| chr12:8697751-8698128 | Common:3; Rare:133 | ||||
| chr12:8914355-8914764 | Common:6; Rare:121 | ||||
| chr12:8949601-8949862 | Common:1; Rare:52 | ||||
| chr12:8949927-8950119 | Common:2; Rare:52 | ||||
| chr12:9115839-9115987 | Common:2; Rare:39 | ||||
| chr12:9116227-9116379 | Rare:23 | ||||
| chr12:10172049-10172261 | Rare:53 | ||||
| chr12:10213216-10213424 | Rare:48 |