| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3077289-3077428 | Common:4; Rare:61 | ||||
| chr12:3753057-3753244 | Common:1; Rare:47 | ||||
| chr12:3873072-3873233 | Rare:47 | ||||
| chr12:4273907-4273926 | Rare:5 | ||||
| chr12:4275444-4275566 | Common:2; Rare:14 | ||||
| chr12:4320943-4321253 | Common:5; Rare:118 | ||||
| chr12:4538436-4538907 | Common:1; Rare:104 | ||||
| chr12:4648982-4649178 | Common:2; Rare:63; Clinvar (benign):2 | ||||
| chr12:4720051-4720471 | Common:3; Rare:86 | ||||
| chr12:6200042-6200446 | Common:4; Rare:112 | ||||
| chr12:6200926-6201059 | Rare:30 | ||||
| chr12:6225274-6225534 | Rare:77 | ||||
| chr12:6309924-6310241 | Common:3; Rare:58 | ||||
| chr12:6310511-6310755 | Common:4; Rare:62 | ||||
| chr12:6317608-6317928 | Common:3; Rare:99 |