chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174172215841722164GTGTGT------5GENIChomozygous769941051
174172352141723522CCAT19GENICpossibly homozygous769941053
174172468941724690CT11GENIChomozygous673011780
174172568041725681GA20GENICpossibly homozygous673011781
174172568141725682GT20GENICpossibly homozygous673011782
174172568941725690AC20GENICpossibly homozygous673011783
174172621341726215AG--11GENIChomozygous769941054
174172667541726676T-24GENIChomozygous769941055
174172673841726739AG27GENIChomozygous673011784
174172768041727681G-12GENICpossibly homozygous769941057
174173079441730795TC26GENIChomozygous673011785