| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32457050-32457081 | Rare:2 | ||||
| chr12:32490819-32491128 | Common:1; Rare:47 | ||||
| chr12:32534935-32534995 | Rare:15 | ||||
| chr12:32564393-32564733 | Rare:61 | ||||
| chr12:32574112-32574319 | Rare:39 | ||||
| chr12:32585583-32585876 | Common:2; Rare:47 | ||||
| chr12:32588040-32588106 | Rare:10 | ||||
| chr12:32699649-32699763 | Common:1; Rare:16 | ||||
| chr12:32702975-32703224 | Common:6; Rare:38 | ||||
| chr12:32708152-32708303 | Rare:31; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:32726779-32726997 | Rare:26 | ||||
| chr12:32727171-32727419 | Rare:46 | ||||
| chr12:32736983-32737161 | Common:1; Rare:41; Clinvar (pathogenic):1 | ||||
| chr12:32741273-32741339 | Common:3; Rare:12 | ||||
| chr12:32742304-32742742 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 |