| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7109168-7109398 | Rare:65 | ||||
| chr12:7130273-7130445 | Common:4; Rare:48 | ||||
| chr12:7189496-7189761 | Common:1; Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:7369313-7369556 | Rare:72 | ||||
| chr12:7749538-7749745 | Common:2; Rare:62 | ||||
| chr12:7935881-7936465 | Common:5; Rare:101 | ||||
| chr12:8032362-8032467 | Rare:30 | ||||
| chr12:8032529-8032819 | Common:5; Rare:87 | ||||
| chr12:8032868-8032976 | Common:1; Rare:22 | ||||
| chr12:8081799-8082498 | Common:4; Rare:184; Clinvar:1 | ||||
| chr12:8082660-8082698 | Rare:10 | ||||
| chr12:8227139-8227287 | Common:3; Rare:25 | ||||
| chr12:8227603-8227715 | Rare:33 | ||||
| chr12:8612755-8613051 | Rare:51; Clinvar (benign):1 | ||||
| chr12:8698502-8698633 | Common:3; Rare:39 |