chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177876390878763909AG21GENIChomozygous111105047
177876414978764150AG18GENIChomozygous111105049
177876416278764163CG17GENIChomozygous111105050
177876427678764277AG16GENIChomozygous111105052
177876619478766195AG18GENIChomozygous111105054
177876670678766707TG13GENIChomozygous111105056
177876671078766711TG13GENIChomozygous119301967
177876671478766715TG14GENICpossibly homozygous119301968
177876671878766719TG23GENICpossibly homozygous119301969
177876676678766767AT14GENICpossibly homozygous119301970
177876677078766771AT14GENICpossibly homozygous119301971
177876704578767046GC22GENIChomozygous111105061
177876770678767707CT20GENIChomozygous111105063
177876906478769065GA11GENIChomozygous111105064
177877124178771242AG17GENIChomozygous111105066
177877131778771318AC26GENIChomozygous111105068
177877133178771332GA30GENIChomozygous111105070
177877166278771663GA13GENIChomozygous111105072
177877257578772576TC30GENIChomozygous111105074
177877285478772855CT19GENIChomozygous111105076
177877495578774956CT25GENIChomozygous111105078
177877671878776719GT20GENIChomozygous111105080
177877733378777334AG25GENIChomozygous111105082
177877781178777812TC18GENICpossibly homozygous111105084
177877808878778089TG16GENIChomozygous111105085
177877882878778829TG15GENIChomozygous111105087
177877890778778908AG17GENIChomozygous111105089
177877937178779372CT26GENIChomozygous111105091
177877965278779653TG31GENIChomozygous111105093
177878010478780105AG19GENIChomozygous111105094
177878164778781648AG27GENIChomozygous111105096
177876673878766739GA14GENICpossibly homozygous129501820
177876761778767617TCC22GENIChomozygous129478470
177876805578768055T21GENIChomozygous129478471
177877756078777572GGTGGTGGTGGT7GENIChomozygous129478472