| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52420231-52420300 | Common:2; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995267-52995812 | Common:4; Rare:227 | ||||
| chr6:53349112-53349341 | Rare:59 | ||||
| chr6:53665600-53665884 | Common:1; Rare:64 | ||||
| chr6:56843061-56843468 | Common:1; Rare:105 | ||||
| chr6:57172539-57172773 | Common:1; Rare:76 | ||||
| chr6:57222274-57222360 | Rare:31 | ||||
| chr6:63572546-63572593 | Rare:13 | ||||
| chr6:69796867-69797109 | Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:70413195-70413545 | Common:2; Rare:102 | ||||
| chr6:73696019-73696249 | Common:1; Rare:58 | ||||
| chr6:75205989-75206319 | Common:1; Rare:80 | ||||
| chr6:75284701-75285032 | Common:1; Rare:98 | ||||
| chr6:75493412-75493934 | Common:3; Rare:95 | ||||
| chr6:75601737-75601902 | Common:1; Rare:55 |