| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377860-45378189 | Common:2; Rare:113 | ||||
| chr6:46015490-46015560 | Rare:22 | ||||
| chr6:46129772-46130171 | Common:5; Rare:127 | ||||
| chr6:46491179-46491363 | Common:2; Rare:53 | ||||
| chr6:46491913-46491984 | Rare:18 | ||||
| chr6:46652779-46653013 | Rare:61 | ||||
| chr6:46921847-46922089 | Common:2; Rare:66 | ||||
| chr6:47477695-47478232 | Common:5; Rare:152; Clinvar:6; Clinvar (benign):7 | ||||
| chr6:49463126-49463401 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52671009-52671138 | Rare:35 | ||||
| chr6:52995267-52995812 | Common:4; Rare:227 | ||||
| chr6:53065278-53065618 | Common:1; Rare:118 | ||||
| chr6:53665622-53665883 | Common:1; Rare:57 | ||||
| chr6:57172464-57172809 | Common:1; Rare:102 | ||||
| chr6:63572218-63572717 | Rare:163 |