| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48903940-48904199 | Common:5; Rare:56 | ||||
| chr12:48904376-48904420 | Rare:12; Clinvar:1 | ||||
| chr12:48957367-48957618 | Common:3; Rare:70 | ||||
| chr12:49018736-49018947 | Common:1; Rare:88 | ||||
| chr12:49059958-49060191 | Rare:65 | ||||
| chr12:49094481-49094528 | Rare:11 | ||||
| chr12:49094530-49095031 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:49102319-49102480 | Common:2; Rare:44 | ||||
| chr12:49110642-49111045 | Rare:90 | ||||
| chr12:49129544-49129858 | Common:4; Rare:65 | ||||
| chr12:49130735-49130912 | Common:4; Rare:69 | ||||
| chr12:49130917-49130988 | Rare:27 | ||||
| chr12:49131299-49131648 | Common:2; Rare:138 | ||||
| chr12:49188488-49188655 | Common:2; Rare:22 | ||||
| chr12:49188972-49189111 | Rare:51; Clinvar:2; Clinvar (benign):2 |