| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:47309859-47310091 | Common:1; Rare:52 | ||||
| chr6:47477520-47478030 | Common:2; Rare:137; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:47478067-47478212 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:49463148-49463443 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284210-52284335 | Rare:36 | ||||
| chr6:52284655-52285142 | Common:3; Rare:152 | ||||
| chr6:52361934-52362166 | Common:2; Rare:75 | ||||
| chr6:52420032-52420458 | Common:3; Rare:176; Clinvar:4; Clinvar (benign):5 | ||||
| chr6:52577047-52577314 | Common:5; Rare:95 | ||||
| chr6:52670990-52671169 | Rare:56 | ||||
| chr6:52993888-52994288 | Common:6; Rare:137 | ||||
| chr6:52994242-52994392 | Rare:44 | ||||
| chr6:52994780-52995100 | Common:1; Rare:69 | ||||
| chr6:52995263-52995616 | Common:4; Rare:138 | ||||
| chr6:53061223-53061623 | Rare:94 |