chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X5638385056383851AG20GENIChomozygous63096926
X5638647256386473AG16GENIChomozygous63096927
X5638649756386498CT19GENIChomozygous63096928
X5638793356387934AG26GENIChomozygous63096929
X5638817756388178TC23GENIChomozygous63096930
X5638928856389289TC21GENIChomozygous63096931
X5639341056393411AT18GENICheterozygous63096934
X5639489956394900TC22GENIChomozygous63096935
X5639539856395399CT23GENIChomozygous63096936
X5639543356395434GA21GENIChomozygous63096937
X5639876356398764CA25GENIChomozygous63096939
X5639888456398885GT17GENIChomozygous63125485
X5639834056398341GA18GENIChomozygous63148287
X5639853356398534GA22GENICpossibly homozygous63125484