| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524748-89524865 | Common:1; Rare:22 | ||||
| chr12:89525995-89526063 | Rare:28 | ||||
| chr12:92145836-92146162 | Common:2; Rare:95 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441855-93442141 | Common:2; Rare:91 | ||||
| chr12:93570228-93570389 | Common:1; Rare:34 | ||||
| chr12:93570827-93571075 | Rare:64 | ||||
| chr12:93571722-93571912 | Common:7; Rare:72 | ||||
| chr12:94459833-94460064 | Common:2; Rare:69 | ||||
| chr12:95003593-95003808 | Common:3; Rare:91; Clinvar (benign):6 | ||||
| chr12:95217377-95217774 | Common:4; Rare:111 | ||||
| chr12:95218113-95218303 | Common:2; Rare:53 | ||||
| chr12:96194220-96194556 | Common:5; Rare:114 | ||||
| chr12:96399346-96399482 | Common:1; Rare:42 | ||||
| chr12:96400541-96400710 | Rare:78 |