| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867341-6867675 | Common:2; Rare:154; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868009-6868318 | Common:6; Rare:107 | ||||
| chr12:6873233-6873471 | Common:3; Rare:69 | ||||
| chr12:6904665-6905067 | Common:2; Rare:91 | ||||
| chr12:6914454-6914603 | Rare:42 | ||||
| chr12:6927521-6928172 | Common:1; Rare:165 | ||||
| chr12:6928189-6928307 | Common:1; Rare:23 | ||||
| chr12:6928329-6928489 | Common:2; Rare:35 | ||||
| chr12:6937419-6937773 | Common:3; Rare:101 | ||||
| chr12:6937895-6938165 | Common:1; Rare:125; Clinvar (benign):1 | ||||
| chr12:6943505-6943864 | Common:6; Rare:190 | ||||
| chr12:6943899-6944303 | Common:12; Rare:344; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:6944312-6944678 | Common:2; Rare:150; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:6946279-6946830 | Common:2; Rare:173 | ||||
| chr12:6970131-6970228 | Rare:29 |