| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31958829-31959206 | Rare:122; Clinvar:8 | ||||
| chr6:32128185-32128488 | Common:3; Rare:82 | ||||
| chr6:32154317-32154513 | Rare:24 | ||||
| chr6:32175985-32176282 | Common:1; Rare:67 | ||||
| chr6:32178082-32178456 | Common:3; Rare:56 | ||||
| chr6:32843851-32844123 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32844476-32844782 | Common:1; Rare:63 | ||||
| chr6:32853660-32853820 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:32853999-32854287 | Common:3; Rare:72 | ||||
| chr6:32968461-32968671 | Common:4; Rare:64 | ||||
| chr6:32969097-32969258 | Common:2; Rare:36 | ||||
| chr6:33200345-33200435 | Rare:22 | ||||
| chr6:33200652-33200974 | Common:3; Rare:93 | ||||
| chr6:33208605-33208834 | Common:3; Rare:71 | ||||
| chr6:33209540-33210054 | Common:1; Rare:88 |