| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56851799-56852121 | Rare:58 | ||||
| chr6:56955166-56955440 | Common:1; Rare:69 | ||||
| chr6:57046618-57046773 | Rare:63 | ||||
| chr6:57089893-57090273 | Rare:150 | ||||
| chr6:57160964-57161151 | Rare:47 | ||||
| chr6:57172529-57172788 | Common:1; Rare:84 | ||||
| chr6:57317404-57317684 | Common:1; Rare:76 | ||||
| chr6:63572263-63572607 | Rare:131 | ||||
| chr6:69796873-69797224 | Common:1; Rare:103; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:70413219-70413573 | Common:2; Rare:97 | ||||
| chr6:70481821-70482021 | Common:1; Rare:45 | ||||
| chr6:73263185-73263306 | Common:4; Rare:30 | ||||
| chr6:73519365-73519665 | Common:1; Rare:73 | ||||
| chr6:73520059-73520165 | Common:1; Rare:47 | ||||
| chr6:73520394-73520638 | Common:1; Rare:103 |