chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117405787974057880AATGT11GENIChomozygous50832157
117405790674057907CT21GENIChomozygous50832158
117405791074057911AG21GENIChomozygous50832159
117405791474057915CG21GENIChomozygous50832160
117406127774061278A-11GENICheterozygous50961780
117406322574063226AACTGAGCCATCTCTCCAGCCC15GENIChomozygous50832162
117406377574063776AAT10GENICpossibly homozygous50832163
117406377574063776AAC10GENICheterozygous50892691
117407849074078491AC15GENIChomozygous50832164
117408231574082316CA26GENICheterozygous50832165
117408243174082432AG32GENICheterozygous50961781
117408244174082442CA25GENICheterozygous50832167
117408252174082522AG20GENICheterozygous50961782
117408296374082964AG24GENICheterozygous50832168
117408299774082998GT12GENIChomozygous50832169
117408499174084995ATTT----3GENIChomozygous50832170
117408703774087038AATCATCTT31GENIChomozygous50832171
117408991874089919T-12GENICheterozygous50961783