chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X117091374117091375GC31GENIChomozygous140688893
X117091659117091659T21GENICpossibly homozygous140594037
X117091716117091717GA23GENIChomozygous140688894
X117092922117092923GA13GENIChomozygous140688895
X117093887117093887AT27GENIChomozygous140594038
X117097950117097951AG27GENIChomozygous140688896
X117098699117098700CT23GENIChomozygous140688897
X117100030117100031CT30GENIChomozygous140688898
X117100253117100254CT20GENIChomozygous140688899
X117103528117103529GT23GENIChomozygous140688900
X117103543117103544CT23GENIChomozygous140688901
X117104047117104048AG29GENIChomozygous140688902
X117104336117104337TC31GENIChomozygous140688903
X117107365117107366GC26GENIChomozygous140688904
X117107480117107481CT23GENIChomozygous140688905