chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124867667948676680GT42GENIChomozygous50228761
124867679248676793AG32GENIChomozygous50228763
124867692248676923GGAAAA4GENIChomozygous50228765
124867733848677339CT42GENIChomozygous50228770
124867796648677967TA31GENIChomozygous50228772
124867916348679164G-20GENIChomozygous50228774
124867997648679977A-1GENIChomozygous50387929
124868057148680572GC26GENIChomozygous50228776
124868063248680638TTTTTG------13GENIChomozygous50228778
124868081448680815CCTTT5GENIChomozygous50228780
124868083348680834GT11GENICheterozygous50228782
124868083448680835GT11GENIChomozygous50228784
124868087348680874TC17GENIChomozygous50228788
124868129548681296CA17GENICpossibly homozygous50343534
124868162248681623CT34GENIChomozygous50228790
124868197348681974CG27GENIChomozygous50228792
124868262048682621CT31GENIChomozygous50228794
124868275148682752TC35GENIChomozygous50228796
124868292048682924GTGT----29GENIChomozygous50228798
124868367248683677TTTTT-----10GENICheterozygous50228800
124868369348683694T-12GENIChomozygous50228802
124868394748683948GA34GENIChomozygous50228804
124868480148684828AGATGGATGGAATCCTAACACCTGGAT---------------------------20GENIChomozygous50228806
124868553148685532GC10GENICheterozygous50228810
124868553748685538CT10GENICheterozygous50228812
124868556748685568AG14GENICheterozygous50228814
124868557148685572CCAT8GENICpossibly homozygous50228816
124868615448686155TC37GENIChomozygous50228818
124868646448686465AG32GENIChomozygous50228820
124868653948686540GA41GENIChomozygous50228822
124868769248687693TC35GENIChomozygous50228824