| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201780868-201780996 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202034483-202034623 | Common:1; Rare:48 | ||||
| chr2:202034942-202035260 | Common:1; Rare:104 | ||||
| chr2:202238468-202238720 | Common:1; Rare:87; Clinvar:1 | ||||
| chr2:202265656-202266009 | Common:2; Rare:133 | ||||
| chr2:202911620-202912279 | Common:3; Rare:159 | ||||
| chr2:203238168-203238396 | Common:2; Rare:48 | ||||
| chr2:203238841-203239057 | Common:2; Rare:88 | ||||
| chr2:203239222-203239382 | Rare:55 | ||||
| chr2:203328043-203328443 | Common:2; Rare:147 | ||||
| chr2:203328537-203328616 | Rare:13 | ||||
| chr2:203402364-203402646 | Common:1; Rare:44 | ||||
| chr2:203535322-203535549 | Common:1; Rare:105 | ||||
| chr2:205682100-205682648 | Rare:133 | ||||
| chr2:205682865-205682899 | Rare:8 |