chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73184754031847541AG10GENIChomozygous115637711
73184879031848791AC25GENIChomozygous115637712
73185097531850976GC25GENIChomozygous115637714
73185355531853556CT13GENIChomozygous118346446
73185356331853564GT9GENIChomozygous115637717
73185443731854438AT16GENIChomozygous115637718
73185526731855268CT15GENIChomozygous118346447
73185685731856858GA15GENIChomozygous118346448
73185787531857876TC12GENIChomozygous115637720
73185824231858243CA8GENIChomozygous115637721
73185851231858513TC20GENIChomozygous118346450
73185927431859275GC14GENIChomozygous115637722
73186046331860464GA22GENIChomozygous115637723
73186122231861223TG19GENIChomozygous118346451
73186255931862560AG24GENIChomozygous115637726
73186675431866755TC18GENIChomozygous115637729
73186758131867582TC5GENIChomozygous118346452
73186816031868161AG23GENIChomozygous115637730
73187100731871008AG10GENIChomozygous115637733
73186925631869257GA27GENIChomozygous126656426
73185248131852482TG12GENICheterozygous126656424
73186601131866012CT7GENIChomozygous126656425