chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2169170721691708AG11GENIChomozygous45809884
X2169352921693530T-7GENICheterozygous45809886
X2169665821696659GA12GENICheterozygous45809888
X2170017721700178TC12GENIChomozygous45809890
X2170657921706580AG8GENIChomozygous45104195
X2170883921708840GA7GENIChomozygous45809892
X2171302021713021TA11GENIChomozygous45809894
X2172003721720038GA9GENICpossibly homozygous45809896
X2172115521721156GA1GENIChomozygous45809898
X2172139721721417ACACACACACACACACACAC--------------------1GENIChomozygous45809900
X2172266021722661CT10GENIChomozygous45809902
X2172655821726559GA15GENIChomozygous45104213
X2172728921727290CCT2GENIChomozygous45104214
X2172999121729992TTA3GENIChomozygous45104222
X2173070021730701AG6GENICheterozygous45809904
X2173183421731835A-2GENIChomozygous45565669
X2173205421732055GGA5GENICheterozygous45104225
X2173474521734746A-3GENICheterozygous45104227
X2173475521734757AA--3GENICheterozygous45104228
X2173540521735406C-10GENIChomozygous45809906