| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:91182601-91182916 | Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:92145837-92146215 | Common:2; Rare:114 | ||||
| chr12:92929095-92929161 | Common:1; Rare:15 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441876-93442178 | Common:2; Rare:97 | ||||
| chr12:93571722-93571902 | Common:6; Rare:68 | ||||
| chr12:94459833-94460064 | Common:2; Rare:69 | ||||
| chr12:95003605-95003830 | Common:3; Rare:94; Clinvar (benign):6 | ||||
| chr12:95073378-95073653 | Common:3; Rare:90 | ||||
| chr12:95217370-95217769 | Common:5; Rare:108 | ||||
| chr12:95218071-95218261 | Common:3; Rare:45 | ||||
| chr12:95474020-95474247 | Common:2; Rare:111 | ||||
| chr12:95548796-95548903 | Common:2; Rare:40 | ||||
| chr12:95858817-95859037 | Common:2; Rare:61 | ||||
| chr12:96400541-96400707 | Rare:77 |