chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75451562654515627TC24GENIChomozygous53927540
75451581454515815AG20GENICpossibly homozygous53927541
75451622654516227GA11GENIChomozygous54655681
75451633054516331TC14GENIChomozygous54655683
75451642654516427GA11GENICpossibly homozygous54655685
75451696554516966CT2GENICheterozygous54655687
75451722354517224TC16GENIChomozygous54655689
75451728954517290GA29GENIChomozygous54655691
75451731454517315GA26GENIChomozygous54655693
75451796954517970CCAG8GENICheterozygous53927542
75451810954518112CTT---7GENICpossibly homozygous53927543
75451812454518125GC4GENIChomozygous54655695
75451913854519139GC13GENICheterozygous54655697
75451953954519540TA16GENICpossibly homozygous54655699
75452049354520494AG18GENIChomozygous54655701
75452177954521780TC28GENIChomozygous53927545
75452181054521811AG14GENICpossibly homozygous54655703
75452186854521869AG21GENIChomozygous54655705
75452196654521967AT9GENICpossibly homozygous54655707
75452239554522396CT18GENIChomozygous54655709
75452267954522680CT9GENICpossibly homozygous54655711
75452306754523068A-8GENIChomozygous53927546
75452595454525955AG21GENICpossibly homozygous53927549
75452650654526507T-12GENIChomozygous54655713