| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99504522-99504680 | Rare:43 | ||||
| chr7:99505103-99505294 | Common:6; Rare:68 | ||||
| chr7:99558513-99558891 | Common:4; Rare:112 | ||||
| chr7:99570483-99570778 | Common:1; Rare:44 | ||||
| chr7:99919487-99919640 | Rare:53 | ||||
| chr7:100015530-100015647 | Common:1; Rare:36 | ||||
| chr7:100049713-100049823 | Rare:43 | ||||
| chr7:100081656-100081856 | Common:2; Rare:57 | ||||
| chr7:100088738-100089113 | Common:2; Rare:105 | ||||
| chr7:100100050-100100265 | Common:1; Rare:103 | ||||
| chr7:100101329-100101756 | Common:1; Rare:168; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100103501-100103639 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr7:100119259-100119763 | Common:1; Rare:157; Clinvar:1 | ||||
| chr7:100122546-100122867 | Common:1; Rare:81 | ||||
| chr7:100148684-100149056 | Common:1; Rare:163 |