chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT19GENIChomozygous892822717
5159590377159590378GA12GENIChomozygous892822718
5159590516159590517AG4GENIChomozygous892822719
5159590543159590544TC8GENIChomozygous892822720
5159590567159590568TC6GENIChomozygous892822721
5159590810159590811GA5GENIChomozygous892822722
5159591041159591042CT25GENIChomozygous892822723
5159591165159591166AG18GENIChomozygous892822724
5159591294159591295GA14GENIChomozygous892822725
5159591492159591493CT10GENICheterozygous892822726
5159591711159591712GA14GENIChomozygous892822727
5159591959159591960CT12GENIChomozygous892822728
5159592241159592242AG21GENIChomozygous892822729
5159592551159592552GA12GENIChomozygous892822730
5159592593159592594GA21GENIChomozygous892822731
5159592713159592714CT11GENIChomozygous892822732
5159593011159593012TA8GENIChomozygous892822733
5159593229159593230AG15GENIChomozygous892822734
5159593316159593317AC11GENIChomozygous892822735
5159594481159594482GA16GENIChomozygous892822736
5159595521159595522GA11GENIChomozygous892822737
5159598268159598269GA12GENIChomozygous892822738
5159599504159599505TC24GENIChomozygous892822739
5159600471159600472TC21GENIChomozygous892822740
5159601143159601144CT22GENIChomozygous892822741
5159601217159601218AG12GENIChomozygous892822742
5159601274159601275AG12GENIChomozygous892822743
5159602018159602019CT6GENIChomozygous892822744