| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95073416-95073653 | Common:2; Rare:82 | ||||
| chr12:95217336-95217886 | Common:6; Rare:145 | ||||
| chr12:95218165-95218318 | Common:2; Rare:36 | ||||
| chr12:95474006-95474191 | Common:2; Rare:87 | ||||
| chr12:95548796-95548924 | Common:3; Rare:46 | ||||
| chr12:95790762-95791085 | Common:2; Rare:80 | ||||
| chr12:95858845-95859073 | Common:1; Rare:64 | ||||
| chr12:96035427-96035749 | Common:3; Rare:78 | ||||
| chr12:96194178-96194421 | Common:6; Rare:82 | ||||
| chr12:96907180-96907450 | Common:1; Rare:91 | ||||
| chr12:98515428-98515788 | Rare:119; Clinvar:2 | ||||
| chr12:98593606-98593790 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:98644731-98645293 | Common:5; Rare:161 | ||||
| chr12:98894038-98894120 | Rare:18 | ||||
| chr12:99154648-99154926 | Common:1; Rare:58 |