chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1569493815694939AG28GENIChomozygous108472319
X1569643515696436A19GENIChomozygous131767883
X1569649715696498AT26GENIChomozygous108369976
X1569651515696516TA24GENIChomozygous108369978
X1569756115697562TC14GENIChomozygous108369980
X1570438215704383TC19GENIChomozygous108369984
X1569802215698022TT4GENIChomozygous133353221
X1570622215706223CT20GENIChomozygous108369986
X1570474015704741A20GENICpossibly homozygous129722721