chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122593874125938742GA30GENIChomozygous50144100
122593883625938837AATGC9GENIChomozygous50144102
122593998025939981CG19GENIChomozygous50144104
122594019925940200CT11GENIChomozygous50144106
122594052125940522GA23GENIChomozygous50484544
122594093525940936TG27GENIChomozygous50144108
122594180225941803TA22GENIChomozygous50144110
122594184725941848AG13GENIChomozygous50144112
122594192925941933AAAG----6GENICheterozygous50144118
122594208725942088TG9GENIChomozygous50144120
122594232925942330TC14GENIChomozygous50144122
122594286625942867TC15GENIChomozygous50144126
122594316625943167CT14GENIChomozygous50144128
122594346025943466AAAAAG------20GENIChomozygous50144130
122594351825943519AG21GENIChomozygous50144132
122594381225943813CT22GENIChomozygous50144136
122594382625943827TA18GENIChomozygous50144138
122594385325943854CA16GENIChomozygous50144140
122594385725943858TC14GENIChomozygous50144142
122594405425944055GA22GENIChomozygous50144150
122594488625944887G-13GENIChomozygous50144152
122594504225945043AC12GENIChomozygous50144154
122594516825945169CA14GENIChomozygous50144156
122594543825945439TA18GENIChomozygous50144158
122594598025945981CA29GENIChomozygous50144160
122594608425946085TC23GENIChomozygous50144162
122594619125946192GGCAGCTCCGCCCAGGCCGC20GENIChomozygous50144164
122594630725946308C-21GENIChomozygous50144166
122594631625946317AC24GENIChomozygous50144168
122594654725946548TA16GENIChomozygous50144170
122594708525947086AT33GENIChomozygous50144172
122594747425947475TC14GENIChomozygous50144174
122594759125947592CT26GENIChomozygous50144176
122594845625948457AG23GENIChomozygous50144178
122594857025948571GA28GENIChomozygous50144180
122594873325948734CT20GENIChomozygous50372617
122594907525949076CT31GENIChomozygous50144182
122594976925949770GA15GENIChomozygous50144188
122595034325950345GA--15GENIChomozygous50144190