chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108548052685480527GA45GENIChomozygous144873128
108548228185482282CT27GENIChomozygous144873129
108548259385482594TC39GENIChomozygous138841298
108548996185489962TC30GENIChomozygous138841307
108549029685490297GC28GENIChomozygous138841308
108549050285490503TA61GENIChomozygous138841309
108549285185492852TA35GENIChomozygous144873130
108549350685493507CG34GENIChomozygous144873131
108549360185493602CT30GENIChomozygous144873132
108549410585494106CT49GENIChomozygous144873133
108549422685494227AC44GENIChomozygous138841313
108549427985494280GA40GENIChomozygous144873134
108549429685494297GA43GENIChomozygous144873135
108549437485494375AG42GENIChomozygous138841314
108549472685494727TC36GENIChomozygous143463177
108549503885495039CT40GENIChomozygous144873136
108549504985495050TA41GENIChomozygous138841317
108549097985490983CTGT27GENIChomozygous144857430
108549516885495185TCCTCCATCCTCCTCCA6GENIChomozygous144857431
108549606285496063AC42GENIChomozygous138841318
108549639485496395CA34GENIChomozygous138841319
108549743185497433TT24GENIChomozygous145148514
108549780585497806TG40GENIChomozygous138841322
108549789085497891TC39GENIChomozygous144873137
108549791885497919AT39GENIChomozygous144873138
108549821885498219C45GENIChomozygous144857434
108549952385499523A27GENICpossibly homozygous138696682
108550035885500359TC23GENIChomozygous138841327
108550043885500439TC42GENIChomozygous138841328
108550063385500634AG37GENIChomozygous138841330
108550064685500647CT40GENIChomozygous144873139
108550121285501213GA48GENIChomozygous138841332
108550133485501335TC41GENIChomozygous138841333
108550246285502463GT40GENIChomozygous138841335
108550247185502472AG41GENIChomozygous138841336
108550290485502905G36GENIChomozygous144857435
108550723885507239AG23GENIChomozygous138841350