chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96576405665764057CT28GENIChomozygous117783167
96576462965764630GA22GENIChomozygous117710292
96576568365765684GA29GENIChomozygous117783168
96576615465766155GA28GENICpossibly homozygous117783169
96576736265767363GA26GENIChomozygous117783170
96577014165770142TC42GENIChomozygous117580072
96577138565771386GA14GENICpossibly homozygous117783171
96577143265771433CA10GENIChomozygous117710296
96577153765771538AG20GENIChomozygous117710298
96577194465771945TG22GENIChomozygous117710300
96577416265774163GA37GENIChomozygous117783172
96577516365775164AG32GENIChomozygous117367451
96577596865775969GA31GENIChomozygous117710312
96577608265776083AG27GENIChomozygous117710314
96577670265776703GT12GENIChomozygous117710316
96577711065777111CT32GENIChomozygous117549137
96577712465777125CT38GENIChomozygous117783173
96577854765778548TC4GENICheterozygous117367453
96578173065781731CT13GENIChomozygous117783174