chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104706689247066893AG11GENIChomozygous874574080
104706720747067208AG15GENIChomozygous874574081
104706738747067388TC16GENIChomozygous874574082
104706760647067607GA14GENIChomozygous874574083
104706850747068508AG21GENIChomozygous874574084
104708237347082374GA13GENIChomozygous874574085
104708275547082756TG8GENIChomozygous874574086
104708308147083082GA14GENIChomozygous874574087
104708367247083673TC22GENIChomozygous874574088
104708446147084462TC28GENIChomozygous874574089
104708510747085108GA22GENIChomozygous874574090
104708587347085874TC11GENIChomozygous874574091
104708642247086423GC23GENIChomozygous874574092
104708650047086501AG14GENIChomozygous874574093
104708655247086553CT12GENIChomozygous874574094
104708665247086653CA7GENIChomozygous874574095
104708734847087349GA23GENIChomozygous874574096
104708819347088194GT13GENIChomozygous874574097
104708996147089962TC15GENICheterozygous874574098
104709123347091234GA19GENIChomozygous874574099
104709128847091289GT13GENIChomozygous874574100
104709132947091330GA23GENIChomozygous874574101
104709153347091534CT25GENIChomozygous874574102
104709296347092964TC28GENIChomozygous874574103
104709340547093406AG17GENIChomozygous874574104
104709370447093705GC9GENIChomozygous874574105
104709370847093709TC9GENIChomozygous874574106
104709382547093826CA28GENIChomozygous874574107
104709496247094963CA15GENICheterozygous874574108
104709540047095401AC27GENIChomozygous874574109
104709650347096504AC22GENIChomozygous874574110
104709698847096989CT12GENIChomozygous874574111
104709700447097005TC17GENIChomozygous874574112
104709781247097813TC8GENIChomozygous874574113
104709799047097991CT13GENIChomozygous874574114
104709839847098399CT23GENIChomozygous874574115
104710080047100801AG5GENIChomozygous874574116
104710113147101132CT8GENIChomozygous874574117
104710175847101759CT22GENIChomozygous874574118
104710346547103466GA19GENIChomozygous874574119