Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:52770916-52771052 | Common:2; Rare:32 | ||||
chr3:53130405-53130523 | Common:1; Rare:39; Clinvar (benign):3 | ||||
chr3:53347518-53347672 | Common:1; Rare:45 | ||||
chr3:53846400-53846577 | Rare:59 | ||||
chr3:53891794-53892050 | Common:2; Rare:80 | ||||
chr3:55766736-55766943 | Rare:35 | ||||
chr3:56557081-56557228 | Common:2; Rare:55 | ||||
chr3:57079257-57079373 | Common:2; Rare:39 | ||||
chr3:57227604-57227913 | Common:3; Rare:106 | ||||
chr3:57556000-57556321 | Rare:80 | ||||
chr3:57597295-57597669 | Common:4; Rare:116 | ||||
chr3:58165297-58165483 | Rare:30 | ||||
chr3:61251308-61251594 | Common:4; Rare:71 | ||||
chr3:62318927-62319049 | Rare:49 | ||||
chr3:62875361-62875468 | Common:1; Rare:20 |