| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89352404-89352707 | Rare:87 | ||||
| chr12:93441901-93442168 | Common:2; Rare:84 | ||||
| chr12:93571766-93571865 | Common:6; Rare:39 | ||||
| chr12:95217377-95217746 | Common:4; Rare:100 | ||||
| chr12:95218055-95218275 | Common:3; Rare:49 | ||||
| chr12:96035562-96035751 | Common:2; Rare:38 | ||||
| chr12:98515518-98515653 | Rare:42; Clinvar:1 | ||||
| chr12:98645018-98645296 | Common:2; Rare:80 | ||||
| chr12:101407731-101408035 | Common:2; Rare:73 | ||||
| chr12:102120073-102120223 | Rare:58 | ||||
| chr12:103930336-103930557 | Common:4; Rare:99 | ||||
| chr12:103965710-103965893 | Common:2; Rare:49 | ||||
| chr12:104064457-104064544 | Rare:21 | ||||
| chr12:109477287-109477650 | Common:3; Rare:89 | ||||
| chr12:109573448-109573813 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 |