chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98142731081427311GA13GENIChomozygous117585125
98142734581427346AT25GENIChomozygous117585127
98142766581427666TG15GENIChomozygous117585129
98142833181428332AG17GENIChomozygous117585135
98142834081428341CA19GENIChomozygous117585137
98142905081429051CT16GENIChomozygous117585141
98142930581429306GT22GENIChomozygous117585143
98142934281429343TC22GENIChomozygous117585145
98142977281429773TC23GENIChomozygous117585147
98143034781430348TC24GENIChomozygous117585149
98143050081430501TG19GENIChomozygous117585151
98143062481430625AC21GENIChomozygous117585153
98143071281430713AG24GENIChomozygous117585157
98143073181430732TC21GENIChomozygous117585159
98143079381430794CT16GENIChomozygous117585161
98143097081430971AG20GENIChomozygous117585163
98143103281431033TG29GENIChomozygous117585165
98143198081431981CT17GENIChomozygous120279434
98143169681431697TA28GENICpossibly homozygous120279432
98143189281431893GA20GENIChomozygous120279433