| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43516791-43517123 | Common:6; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575962-43576190 | Rare:90; Clinvar:4 | ||||
| chr6:43629143-43629410 | Common:2; Rare:83 | ||||
| chr6:43635793-43635893 | Common:1; Rare:28 | ||||
| chr6:43687698-43687848 | Common:1; Rare:61 | ||||
| chr6:43770081-43770230 | Common:2; Rare:45 | ||||
| chr6:43771896-43772034 | Rare:26 | ||||
| chr6:44127278-44127639 | Common:4; Rare:97 | ||||
| chr6:44246890-44247193 | Common:4; Rare:129 | ||||
| chr6:44387447-44387742 | Common:4; Rare:77 | ||||
| chr6:45377624-45377662 | Rare:19 | ||||
| chr6:45377805-45378204 | Common:2; Rare:130 | ||||
| chr6:47478067-47478241 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:49463174-49463433 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284676-52285046 | Common:2; Rare:130 |