| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2890705-2890938 | Common:1; Rare:92 | ||||
| chr12:3873355-3873514 | Common:1; Rare:36 | ||||
| chr12:4320969-4321236 | Common:4; Rare:95 | ||||
| chr12:4648971-4649149 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr12:5431970-5432143 | Common:1; Rare:61 | ||||
| chr12:6493234-6493398 | Common:6; Rare:45 | ||||
| chr12:6493793-6494126 | Common:2; Rare:100 | ||||
| chr12:6534284-6534582 | Common:5; Rare:125 | ||||
| chr12:6536526-6536713 | Rare:68 | ||||
| chr12:6568260-6568357 | Rare:36 | ||||
| chr12:6606363-6606523 | Common:2; Rare:70 | ||||
| chr12:6607389-6607692 | Common:5; Rare:38 | ||||
| chr12:6663102-6663400 | Common:2; Rare:82 | ||||
| chr12:6723844-6724172 | Common:1; Rare:70 | ||||
| chr12:6753055-6753189 | Common:4; Rare:49 |