| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:55579013-55579226 | Rare:74 | ||||
| chr6:56542761-56543034 | Common:2; Rare:47 | ||||
| chr6:56851596-56851672 | Rare:23 | ||||
| chr6:56851877-56852265 | Rare:62 | ||||
| chr6:57046457-57046759 | Rare:107 | ||||
| chr6:57089905-57090200 | Rare:103 | ||||
| chr6:57222274-57222353 | Rare:25 | ||||
| chr6:57317573-57317667 | Rare:30 | ||||
| chr6:62286099-62286355 | Common:1; Rare:79 | ||||
| chr6:63572270-63572675 | Rare:144 | ||||
| chr6:63635547-63635924 | Rare:133 | ||||
| chr6:68634866-68635504 | Common:3; Rare:163 | ||||
| chr6:68635715-68635973 | Rare:50 | ||||
| chr6:69796546-69796662 | Common:1; Rare:23 | ||||
| chr6:69796847-69797151 | Common:1; Rare:94; Clinvar:4; Clinvar (benign):3 |