chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162096281620962817GT52GENIChomozygous111753840
162096285820962859CT51GENIChomozygous111949011
162096423120964232CG57GENIChomozygous111949013
162096452920964530CT43GENIChomozygous111949015
162096507520965076CT41GENIChomozygous111949017
162096516920965170AG51GENIChomozygous111949019
162096563120965632TC56GENIChomozygous111753842
162096617620966177AT30GENICpossibly homozygous111753844
162097155620971557CA54GENICpossibly homozygous111949021
162097270320972704GA45GENIChomozygous111949023
162097316620973167AT43GENICpossibly homozygous111949025
162097431920974320AG34GENIChomozygous111949028
162097516520975166CT29GENIChomozygous111949030
162097694420976945AC56GENIChomozygous111949032
162097751220977513AT32GENICpossibly homozygous111949034
162097937120979372GA32GENIChomozygous111949036
162097946520979466TC40GENIChomozygous111753852
162098199520981996CG36GENIChomozygous111949038
162098265720982658AG53GENICpossibly homozygous111753858
162098377920983780CT31GENIChomozygous111949040
162098762420987625AC35GENIChomozygous111949042
162098818620988187CT37GENIChomozygous111753864
162098823220988233GA36GENIChomozygous111949044
162098840720988408TG42GENIChomozygous111753866
162098873320988734AG43GENIChomozygous111753868
162098989020989891AC41GENIChomozygous111753870
162098992120989922CT48GENIChomozygous111949046
162099200520992006CT35GENICpossibly homozygous111949048
162099310720993108CT39GENIChomozygous111753876
162099351920993520AG35GENIChomozygous111949050
162099394320993944AG50GENIChomozygous111753878
162099445220994453CT21GENIChomozygous111949052
162099578920995790CT56GENIChomozygous111949054
162099604420996045TG51GENIChomozygous111753884
162099856120998562CG48GENIChomozygous111949056
162099876820998769TA35GENIChomozygous111949058
162099972120999722CT50GENIChomozygous112108073
162099966020999661CT45GENICheterozygous112108071
162100005821000059TG42GENIChomozygous111949060