| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43770076-43770222 | Common:2; Rare:44 | ||||
| chr6:44127351-44127639 | Common:4; Rare:81 | ||||
| chr6:45377866-45378169 | Common:2; Rare:105 | ||||
| chr6:47478100-47478232 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:49463257-49463376 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr6:52420101-52420349 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671054-52671149 | Rare:23 | ||||
| chr6:52995259-52995812 | Common:4; Rare:228 | ||||
| chr6:53065385-53065601 | Common:1; Rare:67 | ||||
| chr6:53348882-53349253 | Common:2; Rare:138 | ||||
| chr6:56693290-56693508 | Rare:39 | ||||
| chr6:69796877-69797182 | Common:1; Rare:88; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:75243749-75243963 | Common:1; Rare:93 | ||||
| chr6:75284715-75285022 | Common:1; Rare:91 | ||||
| chr6:75493778-75494038 | Common:1; Rare:47 |