| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52420125-52420326 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52670991-52671175 | Rare:59 | ||||
| chr6:52995326-52995813 | Common:4; Rare:206 | ||||
| chr6:53061789-53061984 | Rare:39 | ||||
| chr6:53065379-53065592 | Common:1; Rare:64 | ||||
| chr6:53348892-53349204 | Common:2; Rare:118 | ||||
| chr6:57046507-57046758 | Rare:88 | ||||
| chr6:57089894-57090206 | Rare:110 | ||||
| chr6:57172197-57172319 | Rare:39 | ||||
| chr6:57172572-57172768 | Common:1; Rare:65 | ||||
| chr6:57317539-57317651 | Rare:31 | ||||
| chr6:62286165-62286369 | Rare:59 | ||||
| chr6:63635606-63635894 | Rare:109 | ||||
| chr6:69796877-69797162 | Common:1; Rare:86; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:70413162-70413573 | Common:2; Rare:125 |