chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87892592478925924C5GENIChomozygous138249943
87892605578926055T6GENIChomozygous138249944
87892613478926135GA8GENIChomozygous138350066
87892669978926700AG30GENIChomozygous138350070
87892627478926275AT16GENIChomozygous138350067
87892627578926276AT16GENIChomozygous138350068
87892649778926498CT16GENIChomozygous138350069
87892673578926736GA28GENIChomozygous138350071
87892696578926965T26GENIChomozygous138249945
87892699878926999AG26GENIChomozygous138350072
87892720278927203AG5GENIChomozygous138350073
87892721978927220GC5GENIChomozygous138350074
87892724978927250GA7GENIChomozygous138350075
87892817478928175TA26GENIChomozygous138350076
87892940678929407GA18GENIChomozygous138350079
87892955978929560GA20GENIChomozygous138350080
87892988678929887AT20GENIChomozygous138350081
87892999478929995AT23GENIChomozygous138350082
87893024978930250GA22GENIChomozygous138350083
87893067078930671GC26GENIChomozygous138350084
87893079078930791GA19GENIChomozygous138350085
87893165678931657GA17GENIChomozygous138350086
87893178678931787CT12GENIChomozygous138350087
87893182778931828AG16GENICpossibly homozygous138350088
87893229778932298TC19GENIChomozygous138350089
87893274178932742AG19GENIChomozygous138350090
87893561478935615A23GENIChomozygous138249946
87893619278936193CT18GENIChomozygous138350094
87893276778932768GA21GENIChomozygous138350091
87893287878932879TG23GENIChomozygous138350092
87893540978935410AG18GENIChomozygous138350093
87893770378937704AG21GENIChomozygous138350095
87893817378938174AG24GENIChomozygous138350096