| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53794579-53794647 | Common:1; Rare:18 | ||||
| chr6:56542702-56543034 | Common:2; Rare:66 | ||||
| chr6:56851796-56852030 | Rare:43 | ||||
| chr6:57046440-57046767 | Rare:115 | ||||
| chr6:57089880-57090265 | Rare:148 | ||||
| chr6:57172451-57172768 | Common:1; Rare:95 | ||||
| chr6:57222266-57222400 | Rare:53 | ||||
| chr6:57317538-57317674 | Rare:41 | ||||
| chr6:63572229-63572622 | Rare:145 | ||||
| chr6:63635676-63636016 | Common:1; Rare:115 | ||||
| chr6:63636045-63636149 | Rare:34 | ||||
| chr6:65707139-65707368 | Common:3; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:68634883-68635499 | Common:3; Rare:158 | ||||
| chr6:69796867-69797184 | Common:1; Rare:93; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:70413174-70413585 | Common:2; Rare:125 |