| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99472646-99473018 | Common:4; Rare:109 | ||||
| chr7:99500179-99500440 | Common:4; Rare:65 | ||||
| chr7:99504868-99505016 | Rare:42 | ||||
| chr7:99551980-99552185 | Rare:68 | ||||
| chr7:99558483-99558929 | Common:5; Rare:136 | ||||
| chr7:99616836-99617012 | Common:2; Rare:62 | ||||
| chr7:99919476-99919651 | Rare:56 | ||||
| chr7:100015489-100015675 | Common:1; Rare:53 | ||||
| chr7:100081685-100081833 | Common:1; Rare:43 | ||||
| chr7:100095362-100095511 | Common:2; Rare:58 | ||||
| chr7:100100467-100100852 | Common:3; Rare:160 | ||||
| chr7:100101314-100101764 | Common:1; Rare:179; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100119255-100119788 | Common:1; Rare:167; Clinvar:1 | ||||
| chr7:100122540-100122907 | Common:1; Rare:94 | ||||
| chr7:100148614-100149047 | Common:1; Rare:184 |