| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57941405-57941688 | Common:3; Rare:83 | ||||
| chr12:59595904-59596196 | Common:5; Rare:69 | ||||
| chr12:62260062-62260439 | Common:1; Rare:143 | ||||
| chr12:62466659-62466826 | Rare:60 | ||||
| chr12:63779720-63780165 | Common:4; Rare:176; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:64222242-64222355 | Rare:39 | ||||
| chr12:64452041-64452171 | Common:1; Rare:47 | ||||
| chr12:64759358-64759479 | Rare:40; Clinvar:3 | ||||
| chr12:65169470-65169588 | Common:1; Rare:41 | ||||
| chr12:65278621-65278756 | Rare:38 | ||||
| chr12:66130711-66130805 | Rare:33 | ||||
| chr12:67648502-67648757 | Common:2; Rare:61 | ||||
| chr12:68610733-68610947 | Rare:91 | ||||
| chr12:68933157-68933366 | Rare:67 | ||||
| chr12:71686026-71686120 | Common:1; Rare:25 |