| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459811-94460053 | Common:3; Rare:69 | ||||
| chr12:95003593-95003831 | Common:3; Rare:99; Clinvar (benign):6 | ||||
| chr12:95073392-95073680 | Common:2; Rare:93 | ||||
| chr12:95217239-95217907 | Common:6; Rare:186 | ||||
| chr12:95218160-95218482 | Common:2; Rare:66 | ||||
| chr12:95474030-95474295 | Common:2; Rare:116 | ||||
| chr12:95548690-95548914 | Common:6; Rare:62 | ||||
| chr12:95858797-95859081 | Common:3; Rare:83 | ||||
| chr12:96035433-96035767 | Common:3; Rare:80 | ||||
| chr12:96399364-96399490 | Common:1; Rare:39 | ||||
| chr12:96489397-96489612 | Common:2; Rare:50 | ||||
| chr12:96907195-96907290 | Rare:37 | ||||
| chr12:98515430-98515814 | Rare:128; Clinvar:4 | ||||
| chr12:98593474-98593870 | Common:2; Rare:124; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644737-98645317 | Common:5; Rare:168 |