| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4273697-4273879 | Common:1; Rare:51 | ||||
| chr12:4275421-4275775 | Common:3; Rare:66 | ||||
| chr12:4278721-4278733 | Rare:3 | ||||
| chr12:4320727-4320816 | Common:2; Rare:26 | ||||
| chr12:4320843-4321418 | Common:8; Rare:205 | ||||
| chr12:4538388-4538934 | Common:3; Rare:135 | ||||
| chr12:4604828-4605222 | Common:6; Rare:139 | ||||
| chr12:4648546-4648726 | Common:4; Rare:32 | ||||
| chr12:4648727-4649193 | Common:3; Rare:117; Clinvar (benign):2 | ||||
| chr12:4649279-4649333 | Rare:11 | ||||
| chr12:4649343-4649399 | Rare:9 | ||||
| chr12:6200180-6200582 | Common:4; Rare:129 | ||||
| chr12:6200607-6200712 | Common:1; Rare:30 | ||||
| chr12:6200724-6200765 | Common:1; Rare:4 | ||||
| chr12:6200897-6201082 | Rare:40 |