| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2877037-2877274 | Rare:77 | ||||
| chr12:2959833-2959944 | Common:1; Rare:30 | ||||
| chr12:4538431-4538935 | Common:3; Rare:115 | ||||
| chr12:4648989-4649149 | Common:2; Rare:52; Clinvar (benign):1 | ||||
| chr12:6451756-6452132 | Common:4; Rare:69 | ||||
| chr12:6493230-6493386 | Common:6; Rare:44 | ||||
| chr12:6493763-6494063 | Common:2; Rare:94 | ||||
| chr12:6534713-6534859 | Common:2; Rare:66 | ||||
| chr12:6549126-6549258 | Common:1; Rare:23 | ||||
| chr12:6568247-6568391 | Rare:56 | ||||
| chr12:6723858-6724309 | Common:2; Rare:97 | ||||
| chr12:6851237-6851495 | Rare:61 | ||||
| chr12:6867477-6867617 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873282-6873476 | Common:2; Rare:56 | ||||
| chr12:6970418-6970993 | Common:4; Rare:182; Clinvar (benign):1 |