chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41725289417252895AG14GENIChomozygous112526998
41725477717254778CT36GENIChomozygous113331008
41726041617260417GA8GENIChomozygous112527064
41726065417260655GA17GENIChomozygous113331018
41726133917261340GT20GENIChomozygous112527076
41726619717266198TA24GENIChomozygous112527128
41726623417266235GT30GENIChomozygous119456317
41726623517266236TG30GENIChomozygous119456318
41726642017266421TC40GENIChomozygous113252028
41726684417266845AG27GENIChomozygous112527130
41726774717267748CA21GENIChomozygous112527132
41726968817269689CT22GENICpossibly homozygous112527134
41726981017269811CA16GENIChomozygous112527136
41726981517269816GT17GENIChomozygous112527138
41727009617270097TG17GENIChomozygous112527140
41727010517270106CT15GENIChomozygous112527142
41727016017270161AG16GENIChomozygous112527144
41727029517270296CT27GENIChomozygous112527146
41727061717270618GA24GENIChomozygous112527148
41727062217270623GA24GENICpossibly homozygous112527150
41727071517270716GT29GENIChomozygous112527152
41727124417271245TC40GENIChomozygous112527154
41727148117271482TC26GENIChomozygous112527156
41727154317271544AG22GENIChomozygous112527158
41727169617271697GA16GENIChomozygous112527160
41727170117271702GA16GENIChomozygous112527162
41727195017271951TG12GENIChomozygous112527166
41727200617272007GA19GENIChomozygous112527168
41727212317272124TA30GENIChomozygous112527170