chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108802681488026815AG60GENIChomozygous144081129
108802941888029419GA57GENIChomozygous144081130
108802986088029861CT54GENIChomozygous144081131
108803089488030895CA24GENIChomozygous144081132
108803093688030937TC35GENICheterozygous154657641
108803145988031460GA51GENIChomozygous144081133
108803309988033100TC61GENIChomozygous144081141
108803157488031575GA44GENIChomozygous144081134
108803160388031604GA43GENIChomozygous144081135
108803207388032074AG39GENIChomozygous144081136
108803230888032309CT50GENIChomozygous144081137
108803264788032648AG61GENIChomozygous144081138
108803271988032720CT56GENIChomozygous144081139
108803272088032721AG56GENIChomozygous144081140
108803276388032763A45GENICpossibly homozygous144077776
108803282988032829GAG54GENIChomozygous144077777
108803093688030937T35GENIChomozygous403294246
108803312488033125GA62GENIChomozygous144081142
108803327288033273GC48GENIChomozygous144081143
108803341888033419AG44GENIChomozygous144081144
108803369288033693AG44GENIChomozygous144081145
108803381588033816CT39GENIChomozygous144081146
108803398288033983TC47GENIChomozygous144081147
108803399688033997CT43GENIChomozygous144081148
108803597188035972TC31GENIChomozygous144081149
108803953888039539C7GENICpossibly homozygous403294247
108803953888039539CA7GENICheterozygous403294248
108804077388040774AC18GENICheterozygous145215919
108804079988040800TA20GENIChomozygous154657647
108804079988040800T20GENICheterozygous403294249
108804079988040800TC20GENICheterozygous403294250
108804320288043203AG39GENIChomozygous144081150
108804346688043468GC3GENIChomozygous144857468
108804351288043513CT4GENICheterozygous144873173
108804590388045904GC56GENIChomozygous144081151
108804650288046503TC53GENIChomozygous144081152
108804722788047228A23GENIChomozygous144077778
108804727388047274AG22GENIChomozygous144081153
108804723688047253ATATAATATATATATAC14GENICheterozygous148918965
108803560188035602TC51GENIChomozygous138843337