chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122593874125938742GA21GENIChomozygous50144100
122593883625938837AATGC5GENIChomozygous50144102
122593998025939981CG14GENIChomozygous50144104
122594019925940200CT16GENIChomozygous50144106
122594052125940522GA15GENIChomozygous50484544
122594093525940936TG21GENIChomozygous50144108
122594180225941803TA16GENIChomozygous50144110
122594184725941848AG10GENIChomozygous50144112
122594192925941933AAAG----3GENIChomozygous50144118
122594208725942088TG7GENIChomozygous50144120
122594232925942330TC12GENIChomozygous50144122
122594286625942867TC17GENIChomozygous50144126
122594316625943167CT5GENIChomozygous50144128
122594346025943466AAAAAG------14GENIChomozygous50144130
122594351825943519AG10GENIChomozygous50144132
122594381225943813CT13GENIChomozygous50144136
122594382625943827TA14GENIChomozygous50144138
122594385325943854CA15GENIChomozygous50144140
122594385725943858TC14GENIChomozygous50144142
122594405425944055GA19GENIChomozygous50144150
122594488625944887G-12GENIChomozygous50144152
122594504225945043AC15GENIChomozygous50144154
122594516825945169CA12GENIChomozygous50144156
122594543825945439TA17GENIChomozygous50144158
122594598025945981CA14GENIChomozygous50144160
122594608425946085TC24GENIChomozygous50144162
122594619125946192GGCAGCTCCGCCCAGGCCGC15GENIChomozygous50144164
122594630725946308C-21GENIChomozygous50144166
122594631625946317AC20GENIChomozygous50144168
122594654725946548TA23GENIChomozygous50144170
122594708525947086AT26GENIChomozygous50144172
122594747425947475TC18GENIChomozygous50144174
122594759125947592CT14GENIChomozygous50144176
122594845625948457AG18GENIChomozygous50144178
122594857025948571GA21GENIChomozygous50144180
122594873325948734CT17GENIChomozygous50372617
122594907525949076CT21GENIChomozygous50144182
122594976925949770GA7GENIChomozygous50144188
122595034325950345GA--31GENIChomozygous50144190