| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6821532-6821880 | Common:3; Rare:86 | ||||
| chr12:6851902-6852174 | Rare:70 | ||||
| chr12:6867403-6867594 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6904636-6904839 | Common:1; Rare:44 | ||||
| chr12:6943535-6943818 | Common:3; Rare:114 | ||||
| chr12:6943938-6944172 | Common:5; Rare:235; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970607-6970966 | Common:4; Rare:110; Clinvar (benign):1 | ||||
| chr12:7018468-7018584 | Common:1; Rare:30 | ||||
| chr12:7130250-7130454 | Common:5; Rare:54 | ||||
| chr12:7189551-7189731 | Rare:66; Clinvar:4 | ||||
| chr12:7936155-7936493 | Common:5; Rare:51 | ||||
| chr12:8227605-8227691 | Rare:24 | ||||
| chr12:8697797-8698128 | Common:2; Rare:116 | ||||
| chr12:8914360-8914757 | Common:6; Rare:117 | ||||
| chr12:8949951-8950099 | Common:1; Rare:43 |