Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:43516891-43517097 | Common:3; Rare:80; Clinvar:2 | ||||
chr6:44127371-44127642 | Common:4; Rare:76 | ||||
chr6:52995313-52995719 | Common:4; Rare:163 | ||||
chr6:53348948-53349222 | Common:1; Rare:78 | ||||
chr6:75284734-75285022 | Common:1; Rare:78 | ||||
chr6:83193220-83193374 | Common:3; Rare:56 | ||||
chr6:87589964-87590154 | Common:1; Rare:76; Clinvar (benign):3 | ||||
chr6:90536677-90536807 | Rare:24 | ||||
chr6:100881281-100881479 | Common:5; Rare:88 | ||||
chr6:109691169-109691315 | Common:1; Rare:35; Clinvar:4; Clinvar (benign):1 | ||||
chr6:110958628-110958772 | Common:2; Rare:57 | ||||
chr6:112087468-112087658 | Rare:54 | ||||
chr6:116254073-116254175 | Common:1; Rare:22 | ||||
chr6:127266822-127266861 | Rare:13 | ||||
chr6:127343346-127343576 | Common:1; Rare:49 |