| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003593-95003829 | Common:3; Rare:98; Clinvar (benign):6 | ||||
| chr12:95073393-95073731 | Common:2; Rare:103 | ||||
| chr12:95217326-95217840 | Common:6; Rare:138 | ||||
| chr12:95218113-95218284 | Common:2; Rare:46 | ||||
| chr12:95231316-95231468 | Rare:26 | ||||
| chr12:95473942-95474330 | Common:2; Rare:157 | ||||
| chr12:95789535-95789726 | Common:1; Rare:31 | ||||
| chr12:95858601-95859076 | Common:4; Rare:123 | ||||
| chr12:95943206-95943393 | Common:1; Rare:32 | ||||
| chr12:95996289-95996466 | Common:2; Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96035479-96035739 | Common:2; Rare:64 | ||||
| chr12:96400541-96400661 | Rare:56 | ||||
| chr12:96907077-96907149 | Common:1; Rare:24 | ||||
| chr12:96907180-96907561 | Common:1; Rare:114 | ||||
| chr12:98515396-98516194 | Common:3; Rare:295; Clinvar:12; Clinvar (benign):10 |