chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
66972127569721276CT56GENIChomozygous54895984
66972272869722729AG51GENIChomozygous54487138
66972386669723867GGAA21GENICheterozygous54487142
66972386669723867GGA21GENICpossibly homozygous54487144
66972457669724577GC47GENIChomozygous54487148
66972490569724906CT46GENIChomozygous54487154
66972662369726624AACAGTCAC33GENIChomozygous54487167
66972686769726868A-19GENICheterozygous54487171
66972687269726873T-8GENIChomozygous54487173
66972689769726898AC10GENIChomozygous54487175
66972690569726906G-13GENIChomozygous54487177
66972690969726910TC15GENIChomozygous54487179
66972691569726916G-13GENIChomozygous54487181
66972691769726918A-13GENIChomozygous54895986
66972790069727901CT45GENIChomozygous54487185
66972823669728237CCT47GENIChomozygous54487189
66972998569729986C-43GENIChomozygous54895988
66973006169730062A-49GENIChomozygous54895990
66973060869730609CA46GENIChomozygous54895992
66973151869731520AG--47GENIChomozygous54487207
66973220469732205GT57GENIChomozygous54895994
66973311769733118CCTTA41GENIChomozygous54487209
66973324169733242GA54GENIChomozygous54895995
66973398269733983TTTC14GENICheterozygous54895997
66973440869734409TG52GENIChomozygous54895999
66973634669736347A-29GENIChomozygous54896001
66973772069737721TTG44GENIChomozygous54487223
66973894069738941AG54GENICpossibly homozygous54487225
66972537369725375AA--1GENIChomozygous55074108