chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148051103480511035TTCC9GENICpossibly homozygous49521032
148051125280511253GC9GENIChomozygous49521034
148051146780511468GA4GENIChomozygous49521036
148051186980511870CT17GENIChomozygous49521038
148051253680512537CA13GENIChomozygous49521040
148051254080512541TC13GENIChomozygous49014036
148051296780512968GA5GENIChomozygous49521042
148051341980513420CT17GENIChomozygous49521044
148051352380513524TC28GENIChomozygous49014038
148051411580514116CT7GENICpossibly homozygous49521046
148051416280514163CT10GENIChomozygous49521048
148051593680515937CT19GENICpossibly homozygous49521050
148051633880516339AG13GENIChomozygous49521052
148051642180516422TG12GENICpossibly homozygous49014043
148051867380518674CT18GENIChomozygous49014044
148051885580518856CA5GENICheterozygous49521056
148051886180518862CA3GENIChomozygous49521058