chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT22GENIChomozygous935168667
5159590355159590356AC22GENIChomozygous935168668
5159590356159590357GC22GENIChomozygous935168669
5159590377159590378GA25GENIChomozygous935168670
5159590516159590517AG14GENIChomozygous935168671
5159590543159590544TC15GENIChomozygous935168672
5159590567159590568TC14GENIChomozygous935168673
5159590810159590811GA19GENIChomozygous935168674
5159591041159591042CT16GENIChomozygous935168675
5159591165159591166AG13GENIChomozygous935168676
5159591294159591295GA18GENIChomozygous935168677
5159591492159591493CT11GENIChomozygous935168678
5159591711159591712GA22GENIChomozygous935168679
5159591959159591960CT11GENIChomozygous935168680
5159592241159592242AG15GENIChomozygous935168681
5159592551159592552GA18GENIChomozygous935168682
5159592593159592594GA20GENIChomozygous935168683
5159592713159592714CT17GENIChomozygous935168684
5159593011159593012TA13GENIChomozygous935168685
5159593229159593230AG17GENIChomozygous935168686
5159593316159593317AC16GENIChomozygous935168687
5159594481159594482GA15GENIChomozygous935168688
5159595521159595522GA20GENIChomozygous935168689
5159598268159598269GA15GENIChomozygous935168690
5159599504159599505TC18GENIChomozygous935168691
5159601143159601144CT25GENIChomozygous935168692
5159601217159601218AG21GENIChomozygous935168693
5159601274159601275AG18GENIChomozygous935168694
5159602018159602019CT6GENIChomozygous935168695