chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162096281620962817GT5GENIChomozygous111753840
162096412920964130TG26GENIChomozygous112220391
162096419420964195TC13GENIChomozygous112053037
162096575620965757TC6GENICheterozygous125684515
162096617620966177AT16GENIChomozygous111753844
162096787420967875TC18GENIChomozygous112053038
162096928320969284CT7GENICheterozygous125684517
162097248720972488AG15GENIChomozygous112053039
162097362920973630GA10GENICheterozygous112220392
162097590820975909CA7GENIChomozygous112053042
162097591420975915GA4GENIChomozygous112053043
162097670420976705AT7GENIChomozygous112053044
162097801920978020GC17GENICpossibly homozygous112053045
162097946520979466TC12GENIChomozygous111753852
162098116320981164GA15GENIChomozygous112053048
162098265720982658AG19GENIChomozygous111753858
162098639620986397GA12GENIChomozygous112053051
162098274620982747GA17GENIChomozygous112053050
162098762420987625AC15GENIChomozygous111949042
162098793920987940CT7GENIChomozygous111753862
162098818620988187CT5GENIChomozygous111753864
162098873320988734AG8GENIChomozygous111753868
162098919120989192TG5GENIChomozygous112053052
162098989020989891AC13GENIChomozygous111753870
162099310720993108CT8GENIChomozygous111753876
162099351920993520AG8GENIChomozygous111949050
162099394320993944AG12GENIChomozygous111753878
162099604420996045TG13GENIChomozygous111753884
162099902920999030TA13GENIChomozygous112053053