| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6868061-6868213 | Common:6; Rare:58 | ||||
| chr12:6870119-6870318 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6873282-6873532 | Common:2; Rare:73 | ||||
| chr12:6904676-6904890 | Rare:47 | ||||
| chr12:6943531-6943831 | Common:4; Rare:132 | ||||
| chr12:6943921-6944172 | Common:9; Rare:250; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970607-6970983 | Common:4; Rare:121; Clinvar (benign):1 | ||||
| chr12:7018461-7018584 | Common:1; Rare:32 | ||||
| chr12:7130250-7130423 | Common:5; Rare:46 | ||||
| chr12:7189519-7189735 | Rare:73; Clinvar:4 | ||||
| chr12:8032542-8032770 | Common:5; Rare:72 | ||||
| chr12:8697774-8698066 | Common:2; Rare:117 | ||||
| chr12:8914358-8914735 | Common:6; Rare:110 | ||||
| chr12:8949570-8949930 | Common:2; Rare:77 | ||||
| chr12:8949955-8950164 | Common:1; Rare:52 |