| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93677224-93677381 | Common:1; Rare:36 | ||||
| chr12:94459811-94460064 | Common:3; Rare:72 | ||||
| chr12:95003664-95003827 | Common:3; Rare:59; Clinvar (benign):3 | ||||
| chr12:95073411-95073710 | Common:2; Rare:99 | ||||
| chr12:95217377-95217769 | Common:4; Rare:106 | ||||
| chr12:95548707-95548931 | Common:6; Rare:64 | ||||
| chr12:95551368-95551582 | Common:4; Rare:38 | ||||
| chr12:95858797-95859054 | Common:2; Rare:77 | ||||
| chr12:96035523-96035854 | Common:2; Rare:73 | ||||
| chr12:96907139-96907295 | Common:1; Rare:55 | ||||
| chr12:98515435-98515759 | Rare:104; Clinvar:2 | ||||
| chr12:98593401-98593749 | Common:2; Rare:124; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:98644938-98645307 | Common:2; Rare:107 | ||||
| chr12:100267039-100267273 | Common:1; Rare:117 | ||||
| chr12:100573557-100573740 | Rare:64 |