chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84783898347838984TC16GENIChomozygous52621142
84783932347839324CCA1GENIChomozygous53382153
84783976947839770GT15GENIChomozygous52621144
84784014347840144CT37GENIChomozygous52621146
84784045747840458AC57GENICpossibly homozygous52621148
84784096047840961GA42GENIChomozygous52621150
84784099247840993GA38GENIChomozygous52621152
84784297347842974CA8GENIChomozygous53382158
84784348147843482AG39GENIChomozygous52621156
84784441947844420GT23GENIChomozygous52621160
84784473347844734GGAAA7GENICheterozygous52621164
84784526747845268TA62GENIChomozygous52621166