| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7108448-7108722 | Common:1; Rare:75 | ||||
| chr12:7109164-7109407 | Rare:71 | ||||
| chr12:7130203-7130483 | Common:5; Rare:71 | ||||
| chr12:7131225-7131358 | Common:1; Rare:20 | ||||
| chr12:7189559-7189891 | Common:5; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:7711195-7711440 | Common:1; Rare:32 | ||||
| chr12:7787685-7787902 | Common:1; Rare:53 | ||||
| chr12:7891061-7891172 | Common:1; Rare:36 | ||||
| chr12:7936147-7936698 | Common:6; Rare:91 | ||||
| chr12:8033451-8033723 | Rare:73 | ||||
| chr12:8227546-8227712 | Rare:44 | ||||
| chr12:8697555-8697647 | Rare:28 | ||||
| chr12:8697769-8698094 | Common:2; Rare:122 | ||||
| chr12:8698100-8698307 | Common:4; Rare:75 | ||||
| chr12:8777651-8777982 | Rare:67 |