chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77115273371152734GC52GENIChomozygous115709863
77115291371152914CG41GENIChomozygous115709864
77115292571152926CT39GENIChomozygous115709865
77115299871152999CG50GENIChomozygous115709866
77115341171153412GA42GENIChomozygous115709867
77115409371154094AG41GENIChomozygous115709868
77115409571154096TC41GENIChomozygous115709869
77115412771154128TC40GENIChomozygous115709870
77115423071154231GA23GENIChomozygous115709871
77115458171154582AT55GENIChomozygous115709872
77115463471154635GA47GENIChomozygous115709873
77115481171154812TG52GENIChomozygous115709874
77115584771155848CT45GENICpossibly homozygous115709875
77115584871155849AG43GENIChomozygous115709876
77115585371155854CT43GENIChomozygous115709877
77115595571155956TA36GENIChomozygous115709878
77115644971156450CT55GENIChomozygous115709879
77115860071158601AG34GENICpossibly homozygous115709880
77116594871165949CA48GENIChomozygous115709881
77116710971167110TA38GENICheterozygous115709882