| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169725720-169726270 | Common:3; Rare:122 | ||||
| chr6:169751400-169751860 | Common:6; Rare:319; Clinvar (benign):10 | ||||
| chr6:170306545-170306824 | Common:4; Rare:165 | ||||
| chr6:170553175-170553354 | Common:4; Rare:153 | ||||
| chr6:170554150-170554476 | Common:3; Rare:172 | ||||
| chr6:170584564-170584790 | Common:3; Rare:148 | ||||
| chr7:194337-194855 | Common:12; Rare:111 | ||||
| chr7:519111-519501 | Common:1; Rare:152 | ||||
| chr7:726577-726775 | Common:1; Rare:147; Clinvar (benign):2 | ||||
| chr7:727216-727377 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:727566-727695 | Rare:24 | ||||
| chr7:815792-816851 | Common:43; Rare:541 | ||||
| chr7:926370-926780 | Common:2; Rare:201 | ||||
| chr7:954601-954760 | Common:2; Rare:39 | ||||
| chr7:975480-975691 | Common:2; Rare:172 |