| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134223930-134224134 | Common:2; Rare:61 | ||||
| chr11:134224533-134224695 | Rare:61 | ||||
| chr11:134225432-134225676 | Rare:69 | ||||
| chr11:134253298-134253601 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:389232-389368 | Rare:53 | ||||
| chr12:389454-389596 | Common:5; Rare:52 | ||||
| chr12:401436-401664 | Rare:63 | ||||
| chr12:610353-610519 | Common:2; Rare:17 | ||||
| chr12:643616-643725 | Rare:19 | ||||
| chr12:752433-752615 | Common:1; Rare:64 | ||||
| chr12:949516-949537 | Common:1; Rare:5 | ||||
| chr12:990504-990586 | Common:1; Rare:26 | ||||
| chr12:991085-991330 | Common:4; Rare:108 | ||||
| chr12:2004420-2004629 | Common:1; Rare:77 | ||||
| chr12:2796919-2797229 | Rare:73 |