chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84783898347838984TC17GENIChomozygous52621142
84783976947839770GT6GENIChomozygous52621144
84784014347840144CT19GENICheterozygous52621146
84784045747840458AC25GENICheterozygous52621148
84784096047840961GA7GENICheterozygous52621150
84784099247840993GA16GENICpossibly homozygous52621152
84784297347842974CA1GENIChomozygous53382158
84784348147843482AG18GENICheterozygous52621156
84784379647843797AG18GENICpossibly homozygous52621158
84784441947844420GT9GENICheterozygous52621160
84784526747845268TA4GENIChomozygous52621166