| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95474005-95474330 | Common:2; Rare:137 | ||||
| chr12:95548774-95548914 | Common:2; Rare:47 | ||||
| chr12:95791128-95791319 | Rare:32 | ||||
| chr12:95858806-95859073 | Common:3; Rare:81 | ||||
| chr12:95943217-95943311 | Rare:18 | ||||
| chr12:95996289-95996581 | Common:4; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:96035361-96035448 | Rare:25 | ||||
| chr12:96035461-96035497 | Rare:10 | ||||
| chr12:96194240-96194556 | Common:5; Rare:105 | ||||
| chr12:96255317-96255511 | Common:1; Rare:38 | ||||
| chr12:96400047-96400095 | Rare:16 | ||||
| chr12:96400437-96400646 | Common:1; Rare:90 | ||||
| chr12:96907190-96907290 | Rare:38 | ||||
| chr12:98515402-98515819 | Common:1; Rare:141; Clinvar:5 | ||||
| chr12:98593494-98593807 | Common:1; Rare:99; Clinvar:4; Clinvar (benign):4 |