| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377873-45378176 | Common:2; Rare:108 | ||||
| chr6:47042251-47042480 | Common:1; Rare:38 | ||||
| chr6:49463188-49463376 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49550519-49550705 | Rare:41 | ||||
| chr6:52284705-52284838 | Common:1; Rare:59 | ||||
| chr6:52995290-52995808 | Common:4; Rare:220 | ||||
| chr6:53348926-53349248 | Common:2; Rare:101 | ||||
| chr6:57046582-57046721 | Rare:46 | ||||
| chr6:57317531-57317647 | Rare:30 | ||||
| chr6:75284740-75285056 | Common:1; Rare:87 | ||||
| chr6:80004357-80004640 | Common:6; Rare:71 | ||||
| chr6:83193222-83193364 | Common:3; Rare:52 | ||||
| chr6:87155268-87155582 | Rare:82 | ||||
| chr6:87589964-87590163 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr6:93419552-93419824 | Common:1; Rare:73 |