chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X117091374117091375GC20GENIChomozygous140688893
X117091659117091659T15GENICpossibly homozygous140594037
X117093887117093887AT14GENIChomozygous140594038
X117097950117097951AG14GENIChomozygous140688896
X117091716117091717GA12GENIChomozygous140688894
X117092922117092923GA8GENICpossibly homozygous140688895
X117098699117098700CT19GENIChomozygous140688897
X117100030117100031CT15GENIChomozygous140688898
X117100253117100254CT18GENIChomozygous140688899
X117103528117103529GT15GENIChomozygous140688900
X117103543117103544CT15GENIChomozygous140688901
X117104047117104048AG10GENIChomozygous140688902
X117104336117104337TC13GENIChomozygous140688903
X117107365117107366GC15GENIChomozygous140688904
X117107480117107481CT10GENIChomozygous140688905