chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71108679211086793TC17GENIChomozygous68595900
71109039911090400AC15GENIChomozygous68595902
71109480411094805CA14GENIChomozygous68595907
71109490311094904GA13GENICpossibly homozygous68595909
71109558811095589GA22GENICpossibly homozygous68595914
71109796511097966GA17GENIChomozygous68595917
71109801611098017GA14GENICpossibly homozygous68595920
71109801711098018GA14GENICpossibly homozygous68595923
71109828711098288AG23GENIChomozygous68595925
71109856311098564AG25GENIChomozygous68595928
71110022611100227CG18GENICheterozygous68595929
71110067411100675CT18GENIChomozygous68595935
71110115311101154CT20GENIChomozygous68595937
71110050211100503GA29GENIChomozygous69716972
71110126311101264CG19GENIChomozygous68595943
71110156711101568AG15GENICpossibly homozygous68595960
71110157811101579CT15GENICpossibly homozygous68595963
71110187911101880GA15GENIChomozygous69716975
71110157511101576CA15GENICpossibly homozygous82085802