chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X5493901454939015TC16GENIChomozygous45302456
X5493913254939133GC21GENIChomozygous45302457
X5493921754939219GG--16GENICpossibly homozygous45302458
X5493921954939220GT15GENICheterozygous45302459
X5493954154939542GA10GENIChomozygous45302460
X5493962254939623GA13GENIChomozygous45302461
X5493971854939719AC23GENIChomozygous45302462
X5493973954939740CCTG19GENIChomozygous45302463
X5493995254939953CT10GENIChomozygous45302464
X5494030254940303GT7GENIChomozygous45302465
X5494050454940505GA7GENIChomozygous45302466
X5494068354940684CCT4GENIChomozygous45302467
X5494069454940695AAAAG2GENIChomozygous45302468
X5494079554940796GA13GENIChomozygous45302469
X5494089354940894GC11GENIChomozygous45302470
X5494093854940939CT15GENIChomozygous45302471
X5494097554940976TA16GENIChomozygous45302472
X5494113454941135TC7GENIChomozygous45302473