| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:70413222-70413573 | Common:2; Rare:97 | ||||
| chr6:73263163-73263286 | Common:3; Rare:31 | ||||
| chr6:73696019-73696207 | Common:1; Rare:37 | ||||
| chr6:75243749-75243963 | Common:1; Rare:93 | ||||
| chr6:75284731-75285020 | Common:1; Rare:81 | ||||
| chr6:75493778-75493899 | Common:1; Rare:27 | ||||
| chr6:78867481-78867621 | Rare:70 | ||||
| chr6:79234587-79234734 | Common:1; Rare:42 | ||||
| chr6:79234736-79234764 | Common:1; Rare:5 | ||||
| chr6:79537394-79537658 | Common:1; Rare:77; Clinvar:2 | ||||
| chr6:81752660-81752785 | Rare:61 | ||||
| chr6:83193222-83193395 | Common:3; Rare:62 | ||||
| chr6:87155229-87155595 | Rare:97 | ||||
| chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:89080571-89080759 | Common:1; Rare:83 |