chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98142731081427311GA42GENICpossibly homozygous117585125
98142734581427346AT39GENIChomozygous117585127
98142766581427666TG42GENICpossibly homozygous117585129
98142817981428180TC40GENICheterozygous117585131
98142818181428182TC38GENICheterozygous117585133
98142833181428332AG41GENIChomozygous117585135
98142834081428341CA42GENIChomozygous117585137
98142856281428563GA33GENIChomozygous117585139
98142905081429051CT54GENICpossibly homozygous117585141
98142930581429306GT52GENIChomozygous117585143
98142934281429343TC63GENIChomozygous117585145
98142977281429773TC51GENICpossibly homozygous117585147
98143034781430348TC51GENIChomozygous117585149
98143050081430501TG44GENICpossibly homozygous117585151
98143062481430625AC49GENIChomozygous117585153
98143063981430640AC49GENICpossibly homozygous117585155
98143071281430713AG56GENIChomozygous117585157
98143073181430732TC63GENIChomozygous117585159
98143079381430794CT71GENIChomozygous117585161
98143097081430971AG50GENIChomozygous117585163
98143103281431033TG50GENIChomozygous117585165
98143212081432121GA44GENIChomozygous117585167
98143268381432684TG49GENICpossibly homozygous117585169
98143342481433425CT47GENIChomozygous117585171