Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:33425656-33425863 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr6:35016829-35017031 | Common:2; Rare:29 | ||||
chr6:35346926-35347098 | Rare:35 | ||||
chr6:35590649-35590991 | Common:1; Rare:58 | ||||
chr6:35601633-35601702 | Rare:9 | ||||
chr6:35687921-35688006 | Rare:20 | ||||
chr6:35727576-35727754 | Common:1; Rare:34 | ||||
chr6:35731336-35731619 | Common:1; Rare:67 | ||||
chr6:35732073-35732087 | Rare:3 | ||||
chr6:36680149-36680219 | Rare:10 | ||||
chr6:37169326-37169528 | Common:4; Rare:38 | ||||
chr6:37173851-37173986 | Rare:34 | ||||
chr6:44249412-44249834 | Common:1; Rare:113 | ||||
chr6:44251284-44251608 | Common:2; Rare:92 | ||||
chr6:44251724-44252159 | Common:2; Rare:150 |