chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122593874125938742GA32GENIChomozygous50144100
122593883625938837AATGC21GENIChomozygous50144102
122593998025939981CG19GENIChomozygous50144104
122594019925940200CT33GENIChomozygous50144106
122594052125940522GA30GENIChomozygous50484544
122594093525940936TG31GENIChomozygous50144108
122594180225941803TA15GENICpossibly homozygous50144110
122594184725941848AG8GENICpossibly homozygous50144112
122594192925941933AAAG----9GENICheterozygous50144118
122594208725942088TG32GENIChomozygous50144120
122594232925942330TC27GENIChomozygous50144122
122594286625942867TC29GENIChomozygous50144126
122594316625943167CT22GENIChomozygous50144128
122594346025943466AAAAAG------32GENIChomozygous50144130
122594351825943519AG31GENIChomozygous50144132
122594381225943813CT27GENIChomozygous50144136
122594382625943827TA26GENIChomozygous50144138
122594385325943854CA29GENIChomozygous50144140
122594385725943858TC30GENIChomozygous50144142
122594405425944055GA31GENIChomozygous50144150
122594488625944887G-18GENIChomozygous50144152
122594504225945043AC31GENIChomozygous50144154
122594516825945169CA27GENIChomozygous50144156
122594543825945439TA20GENIChomozygous50144158
122594598025945981CA30GENICpossibly homozygous50144160
122594608425946085TC19GENIChomozygous50144162
122594619125946192GGCAGCTCCGCCCAGGCCGC27GENIChomozygous50144164
122594630725946308C-24GENIChomozygous50144166
122594631625946317AC23GENIChomozygous50144168
122594654725946548TA25GENIChomozygous50144170
122594708525947086AT34GENICpossibly homozygous50144172
122594747425947475TC24GENIChomozygous50144174
122594759125947592CT27GENIChomozygous50144176
122594845625948457AG21GENIChomozygous50144178
122594857025948571GA18GENIChomozygous50144180
122594907525949076CT40GENIChomozygous50144182
122594976925949770GA25GENIChomozygous50144188
122595034325950345GA--20GENIChomozygous50144190