chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT16GENIChomozygous982300796
5159590355159590356AC16GENIChomozygous982300797
5159590356159590357GC16GENIChomozygous982300798
5159590377159590378GA22GENIChomozygous982300799
5159590516159590517AG10GENIChomozygous982300800
5159590543159590544TC10GENIChomozygous982300801
5159590567159590568TC10GENIChomozygous982300802
5159590810159590811GA15GENIChomozygous982300803
5159591041159591042CT17GENIChomozygous982300804
5159591165159591166AG23GENIChomozygous982300805
5159591294159591295GA23GENIChomozygous982300806
5159591492159591493CT15GENIChomozygous982300807
5159591711159591712GA11GENIChomozygous982300808
5159591959159591960CT14GENIChomozygous982300809
5159592241159592242AG28GENIChomozygous982300810
5159592551159592552GA24GENIChomozygous982300811
5159592593159592594GA22GENIChomozygous982300812
5159592713159592714CT11GENIChomozygous982300813
5159593011159593012TA17GENIChomozygous982300814
5159593229159593230AG22GENIChomozygous982300815
5159593316159593317AC15GENIChomozygous982300816
5159594481159594482GA34GENIChomozygous982300817
5159595521159595522GA21GENIChomozygous982300818
5159598268159598269GA26GENIChomozygous982300819
5159599504159599505TC15GENIChomozygous982300820
5159601143159601144CT16GENIChomozygous982300821
5159601217159601218AG14GENIChomozygous982300822
5159601274159601275AG27GENIChomozygous982300823
5159602018159602019CT4GENIChomozygous982300824