| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106325551-106325916 | Common:1; Rare:126 | ||||
| chr6:106629457-106629620 | Common:1; Rare:35 | ||||
| chr6:108074572-108074866 | Common:1; Rare:102; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr6:108260764-108261040 | Rare:118 | ||||
| chr6:108560714-108560984 | Rare:113 | ||||
| chr6:109009405-109009689 | Common:2; Rare:84 | ||||
| chr6:109094433-109094571 | Rare:31 | ||||
| chr6:109094820-109095551 | Common:6; Rare:187 | ||||
| chr6:109382064-109382198 | Common:4; Rare:54 | ||||
| chr6:109382239-109382268 | Rare:11 | ||||
| chr6:109382270-109382596 | Common:5; Rare:135; Clinvar (benign):2 | ||||
| chr6:109440598-109440887 | Common:2; Rare:100 | ||||
| chr6:109455702-109455865 | Common:2; Rare:49 | ||||
| chr6:109483174-109483258 | Rare:33 | ||||
| chr6:109691028-109691339 | Common:4; Rare:75; Clinvar:4; Clinvar (benign):3 |