Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:46689521-46689700 | Common:2; Rare:75; Clinvar (benign):2 | ||||
chr16:46973620-46973781 | Rare:74 | ||||
chr16:47461041-47461365 | Common:2; Rare:118; Clinvar (benign):2 | ||||
chr16:53054805-53055048 | Common:2; Rare:58 | ||||
chr16:53703814-53704215 | Common:1; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
chr16:54286722-54287005 | Common:1; Rare:86 | ||||
chr16:55479037-55479214 | Rare:42 | ||||
chr16:56451307-56451615 | Common:1; Rare:102 | ||||
chr16:56608429-56608756 | Common:3; Rare:97 | ||||
chr16:56625618-56625838 | Rare:69 | ||||
chr16:56729975-56730185 | Common:1; Rare:47 | ||||
chr16:56931885-56932168 | Common:3; Rare:133 | ||||
chr16:56989459-56989567 | Common:1; Rare:20; Clinvar:1 | ||||
chr16:57185823-57186390 | Common:3; Rare:165 | ||||
chr16:57244964-57245367 | Common:3; Rare:138 |