| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75284679-75285022 | Common:1; Rare:103 | ||||
| chr6:75493531-75493918 | Common:2; Rare:76 | ||||
| chr6:75601730-75601893 | Common:1; Rare:56 | ||||
| chr6:75602235-75602556 | Common:1; Rare:99 | ||||
| chr6:75749022-75749298 | Common:5; Rare:95; Clinvar:3 | ||||
| chr6:79078273-79078586 | Common:1; Rare:126 | ||||
| chr6:79234565-79234968 | Common:4; Rare:92 | ||||
| chr6:79537340-79537658 | Common:2; Rare:99; Clinvar:4 | ||||
| chr6:83193194-83193397 | Common:3; Rare:69 | ||||
| chr6:84764585-84764791 | Rare:60 | ||||
| chr6:85449974-85450105 | Common:1; Rare:36 | ||||
| chr6:85643817-85644107 | Common:2; Rare:88 | ||||
| chr6:87155240-87155588 | Rare:92 | ||||
| chr6:87589946-87590163 | Common:2; Rare:98; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:88963585-88963830 | Common:2; Rare:83 |