chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X153555542153555543TG12GENIChomozygous995761061
X153598807153598808GA17GENIChomozygous995761062
X153598810153598811CA17GENIChomozygous995761063
X153598870153598871CA7GENIChomozygous995761064
X153602136153602137CT9GENIChomozygous995761065
X153602157153602158CT7GENIChomozygous995761066
X153602220153602221CT9GENIChomozygous995761067
X153646535153646536GA6GENIChomozygous995761068
X153646544153646545GA7GENIChomozygous995761069
X153692285153692286GC12GENIChomozygous995761070
X153730942153730943TA18GENICheterozygous995761071
X153731007153731008TA16GENICheterozygous995761072
X153772165153772166GT10GENIChomozygous995761073
X153803100153803101TC9GENICpossibly homozygous995761074
X153836513153836514TG11GENIChomozygous995761075