| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:53065379-53065614 | Common:1; Rare:71 | ||||
| chr6:53348868-53349222 | Common:2; Rare:140 | ||||
| chr6:53665663-53665905 | Common:1; Rare:54 | ||||
| chr6:54018886-54019026 | Common:1; Rare:39 | ||||
| chr6:55579013-55579256 | Common:1; Rare:82 | ||||
| chr6:56843681-56843939 | Common:9; Rare:56 | ||||
| chr6:57046507-57046767 | Rare:91 | ||||
| chr6:57172217-57172798 | Common:1; Rare:170 | ||||
| chr6:57222266-57222391 | Rare:51 | ||||
| chr6:62286151-62286340 | Rare:56 | ||||
| chr6:63572265-63572566 | Rare:113 | ||||
| chr6:63635649-63635903 | Rare:99 | ||||
| chr6:63636044-63636149 | Rare:34 | ||||
| chr6:69796546-69796847 | Common:3; Rare:87 | ||||
| chr6:69796853-69797174 | Common:1; Rare:101; Clinvar:6; Clinvar (benign):3 |