chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X5638371056383711TC15GENIChomozygous63096925
X5638385056383851AG9GENIChomozygous63096926
X5638647256386473AG16GENIChomozygous63096927
X5638649756386498CT12GENIChomozygous63096928
X5638793356387934AG16GENIChomozygous63096929
X5638817756388178TC20GENIChomozygous63096930
X5638928856389289TC9GENIChomozygous63096931
X5639068256390683CA26GENIChomozygous63096932
X5639284656392847GA8GENIChomozygous63096933
X5639341056393411AT8GENIChomozygous63096934
X5639489956394900TC10GENIChomozygous63096935
X5639539856395399CT15GENIChomozygous63096936
X5639543356395434GA10GENIChomozygous63096937
X5639827556398276AC19GENICpossibly homozygous63096938
X5639876356398764CA10GENIChomozygous63096939
X5639893356398934CG15GENIChomozygous63096940
X5639893656398937AT15GENIChomozygous63096941
X5639719756397198TG11GENIChomozygous62955305