chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186016268660162687GA24GENIChomozygous110367619
186016306760163068CT18GENIChomozygous110367621
186016500960165010CT7GENIChomozygous110367627
186016517460165175CT28GENIChomozygous110367629
186016541260165413CT19GENIChomozygous110367631
186016695160166952CT28GENIChomozygous110367643
186016631060166311CG21GENIChomozygous110367637
186016631260166313AC21GENIChomozygous110367639
186016646760166468TG21GENIChomozygous110367641
186017441260174413GA37GENICpossibly homozygous110480737
186017917360179174AT18GENICheterozygous110480739
186018471160184712TC11GENIChomozygous110367647
186018486960184870TC17GENIChomozygous110367649
186018577360185774GT32GENIChomozygous110367651
186018577460185775AG32GENIChomozygous110367653
186018583060185831CT30GENIChomozygous110367656
186020182160201822CT28GENIChomozygous110367660
186021732960217330AT22GENIChomozygous110367662
186021811160218112TG19GENIChomozygous110367664
186021819860218199TC18GENIChomozygous110367667
186021826760218268TC22GENIChomozygous110367669
186021826860218269GA23GENIChomozygous110367671
186021993560219936TC20GENIChomozygous110367673
186022099560220996CA19GENIChomozygous110367675
186022138060221381CA33GENIChomozygous110367677
186022321860223219CT29GENIChomozygous110367679
186022421360224214AG6GENIChomozygous110367681