chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87892592478925924C7GENIChomozygous138249943
87892605578926055T12GENIChomozygous138249944
87892613478926135GA11GENIChomozygous138350066
87892627478926275AT19GENIChomozygous138350067
87892627578926276AT19GENIChomozygous138350068
87892649778926498CT25GENIChomozygous138350069
87892669978926700AG22GENIChomozygous138350070
87892673578926736GA23GENICpossibly homozygous138350071
87892696578926965T19GENIChomozygous138249945
87892699878926999AG19GENIChomozygous138350072
87892720278927203AG9GENICpossibly homozygous138350073
87892721978927220GC13GENICpossibly homozygous138350074
87892724978927250GA12GENIChomozygous138350075
87892817478928175TA21GENIChomozygous138350076
87892906378929064CT6GENIChomozygous138350077
87892906478929065AG6GENIChomozygous138350078
87892940678929407GA21GENIChomozygous138350079
87892955978929560GA18GENIChomozygous138350080
87892988678929887AT19GENIChomozygous138350081
87892999478929995AT24GENIChomozygous138350082
87893024978930250GA16GENIChomozygous138350083
87893067078930671GC25GENIChomozygous138350084
87893079078930791GA11GENIChomozygous138350085
87893165678931657GA20GENIChomozygous138350086
87893178678931787CT13GENIChomozygous138350087
87893182778931828AG15GENIChomozygous138350088
87893287878932879TG17GENIChomozygous138350092
87893274178932742AG14GENIChomozygous138350090
87893229778932298TC18GENIChomozygous138350089
87893276778932768GA13GENIChomozygous138350091
87893540978935410AG22GENIChomozygous138350093
87893561478935615A14GENIChomozygous138249946
87893619278936193CT33GENIChomozygous138350094
87893770378937704AG25GENIChomozygous138350095
87893817378938174AG19GENIChomozygous138350096