chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84783898347838984TC27GENIChomozygous52621142
84783976947839770GT30GENIChomozygous52621144
84784014347840144CT40GENIChomozygous52621146
84784045747840458AC41GENIChomozygous52621148
84784096047840961GA45GENIChomozygous52621150
84784099247840993GA52GENICpossibly homozygous52621152
84784297347842974C-25GENIChomozygous52621154
84784348147843482AG46GENIChomozygous52621156
84784379647843797AG21GENICpossibly homozygous52621158
84784441947844420GT39GENIChomozygous52621160
84784473347844734GGAA21GENICheterozygous52621162
84784473347844734GGAAA21GENICheterozygous52621164
84784526747845268TA31GENIChomozygous52621166