| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95858803-95859077 | Common:5; Rare:153 | ||||
| chr12:95942790-95943380 | Common:5; Rare:188 | ||||
| chr12:96035533-96035755 | Common:2; Rare:48 | ||||
| chr12:96399329-96399441 | Common:1; Rare:37 | ||||
| chr12:96399361-96400282 | Common:4; Rare:296 | ||||
| chr12:96400299-96400704 | Common:3; Rare:222 | ||||
| chr12:96906991-96907524 | Common:5; Rare:258 | ||||
| chr12:98515394-98515850 | Common:1; Rare:273; Clinvar:8 | ||||
| chr12:98516166-98516653 | Common:3; Rare:191 | ||||
| chr12:98593461-98593817 | Common:3; Rare:205; Clinvar:8; Clinvar (benign):8 | ||||
| chr12:98644539-98644870 | Common:6; Rare:160 | ||||
| chr12:98644911-98645329 | Common:6; Rare:221 | ||||
| chr12:100142836-100143062 | Common:5; Rare:145 | ||||
| chr12:100199708-100200330 | Common:5; Rare:201 | ||||
| chr12:100200657-100200883 | Common:1; Rare:123 |