Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:105179864-105180118 | Common:5; Rare:72 | ||||
chr6:106629443-106629681 | Common:4; Rare:57 | ||||
chr6:107490433-107490590 | Common:3; Rare:55 | ||||
chr6:107958088-107958393 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
chr6:108294786-108295077 | Common:1; Rare:79 | ||||
chr6:108560202-108560384 | Rare:57 | ||||
chr6:108560730-108560960 | Rare:96 | ||||
chr6:109009396-109009689 | Common:2; Rare:86 | ||||
chr6:109094038-109094519 | Rare:109 | ||||
chr6:109094521-109094593 | Rare:14 | ||||
chr6:109094827-109095195 | Common:5; Rare:112 | ||||
chr6:109095396-109095557 | Rare:35 | ||||
chr6:109382217-109382517 | Common:3; Rare:143; Clinvar (benign):2 | ||||
chr6:109440582-109440754 | Rare:56 | ||||
chr6:109455666-109456074 | Common:3; Rare:107 |