| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48927270-48928150 | Common:2; Rare:158 | ||||
| chr12:48940830-48941451 | Common:7; Rare:179 | ||||
| chr12:48969870-48970130 | Common:1; Rare:77 | ||||
| chr12:48979630-48980437 | Rare:241; Clinvar (pathogenic):1 | ||||
| chr12:48997125-48997870 | Common:2; Rare:321 | ||||
| chr12:48998137-48998373 | Rare:80 | ||||
| chr12:49019697-49020097 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49055894-49056267 | Rare:118 | ||||
| chr12:49057910-49058310 | Rare:116 | ||||
| chr12:49060530-49060994 | Common:4; Rare:407 | ||||
| chr12:49088250-49088590 | Common:1; Rare:62 | ||||
| chr12:49138630-49138940 | Rare:45 | ||||
| chr12:49160560-49160900 | Common:4; Rare:53 | ||||
| chr12:49161240-49161793 | Common:4; Rare:254 | ||||
| chr12:49233041-49233479 | Common:6; Rare:85 |