| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2877051-2877262 | Rare:64 | ||||
| chr12:2959833-2959944 | Common:1; Rare:30 | ||||
| chr12:4538431-4538934 | Common:3; Rare:115 | ||||
| chr12:4649016-4649171 | Common:2; Rare:53; Clinvar (benign):2 | ||||
| chr12:5431931-5432158 | Common:4; Rare:88 | ||||
| chr12:5432926-5433023 | Rare:25 | ||||
| chr12:6451785-6452149 | Common:4; Rare:69 | ||||
| chr12:6493234-6493398 | Common:6; Rare:45 | ||||
| chr12:6493793-6494133 | Common:2; Rare:103 | ||||
| chr12:6549098-6549270 | Common:1; Rare:32 | ||||
| chr12:6568224-6568402 | Rare:68 | ||||
| chr12:6581060-6581350 | Rare:106; Clinvar (pathogenic):1 | ||||
| chr12:6581360-6581672 | Common:1; Rare:115 | ||||
| chr12:6689373-6689735 | Common:3; Rare:93 | ||||
| chr12:6723855-6724299 | Common:2; Rare:93 |