| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56541324-56541526 | Rare:32 | ||||
| chr6:56542632-56543078 | Common:2; Rare:95 | ||||
| chr6:56642860-56643253 | Rare:69; Clinvar:1 | ||||
| chr6:57172528-57172798 | Common:1; Rare:86 | ||||
| chr6:57222001-57222400 | Rare:138 | ||||
| chr6:57317347-57317651 | Common:2; Rare:70 | ||||
| chr6:62286012-62286355 | Common:2; Rare:105 | ||||
| chr6:63572265-63572610 | Rare:131 | ||||
| chr6:63635676-63636016 | Common:1; Rare:115 | ||||
| chr6:63636044-63636149 | Rare:34 | ||||
| chr6:68635131-68635361 | Common:1; Rare:72 | ||||
| chr6:69796546-69796652 | Common:1; Rare:18 | ||||
| chr6:69796706-69796727 | Common:1; Rare:5 | ||||
| chr6:69796856-69797110 | Rare:84; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70413222-70413613 | Common:2; Rare:110 |