chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73219400032194001CT1GENIChomozygous548577905
73219536932195370CT10GENICpossibly homozygous548577906
73219553932195540CT9GENICheterozygous548577907
73219556732195568TC18GENICpossibly homozygous548577908
73219566232195663TC8GENIChomozygous548577909
73219576532195766GA11GENIChomozygous548577910
73219586632195867CG8GENIChomozygous548577911
73219592532195926TTCAG3GENIChomozygous699046006
73219603132196032CT13GENIChomozygous548577912
73219824832198249TA1GENIChomozygous548577913
73219827232198273TA8GENIChomozygous548577914
73219829132198292CA8GENIChomozygous548577915
73219837832198379TA3GENIChomozygous547303565
73220000732200008CT21GENICpossibly homozygous548577916
73220032632200327AG16GENIChomozygous548577917
73220036732200368TC19GENIChomozygous548577918
73221918332219184TC11GENIChomozygous547303566
73222425832224259GA24GENIChomozygous548577919
73222538832225389AG14GENICpossibly homozygous548577920
73222539932225400TC11GENIChomozygous548577921
73222541832225419CT16GENIChomozygous548577922
73222555832225559GC24GENIChomozygous548577923