| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93571766-93571902 | Common:6; Rare:56 | ||||
| chr12:94459811-94460062 | Common:3; Rare:72 | ||||
| chr12:94616070-94616105 | Rare:7 | ||||
| chr12:95003644-95003806 | Common:3; Rare:63; Clinvar (benign):3 | ||||
| chr12:95073403-95073655 | Common:2; Rare:85 | ||||
| chr12:95217384-95217769 | Common:4; Rare:105 | ||||
| chr12:95473997-95474191 | Common:2; Rare:89 | ||||
| chr12:95548791-95548914 | Common:2; Rare:43 | ||||
| chr12:95858817-95859076 | Common:3; Rare:77 | ||||
| chr12:96907316-96907439 | Common:1; Rare:34 | ||||
| chr12:98515475-98515653 | Rare:56; Clinvar:1 | ||||
| chr12:98644737-98645296 | Common:5; Rare:162 | ||||
| chr12:100200710-100200834 | Rare:37 | ||||
| chr12:100267054-100267414 | Common:1; Rare:148 | ||||
| chr12:100573501-100573763 | Rare:83 |