chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44301710243017103GA23GENIChomozygous56850119
44301723143017232AC24GENIChomozygous56850120
44301737343017374TTTAAA8GENIChomozygous56850121
44301798943017990TC32GENIChomozygous56850122
44301910243019103CA8GENIChomozygous56850124
44301943343019434AC24GENIChomozygous56850125
44301958943019590GC13GENIChomozygous56850126
44301986743019868TC21GENIChomozygous56850127
44301987743019878AG20GENIChomozygous56850128
44302001443020015T-7GENIChomozygous56850129
44302049343020494CT19GENIChomozygous56850130
44302067843020679GGT13GENIChomozygous56850131
44302089843020899AT20GENIChomozygous56850132
44302105543021057GG--14GENICheterozygous56850133
44302106243021063GGT15GENICheterozygous56850134
44302106743021068GGTTTTGTTTTGTTTTTGT14GENIChomozygous56850135
44302107343021074T-17GENICheterozygous56850136
44302137843021379CT11GENIChomozygous56850137
44302153543021536GA16GENIChomozygous56850138
44302157943021580GT15GENIChomozygous56850139
44302203243022033TC15GENIChomozygous56850140
44302206543022066TC17GENIChomozygous56850141
44302207443022075CCT15GENIChomozygous56850142