chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129501912129501913GA16GENIChomozygous54108861
7129501942129501943AG21GENIChomozygous54108862
7129502043129502044TTCACACGCACA19GENIChomozygous54108863
7129502762129502763AG28GENIChomozygous54108864
7129503510129503511GT27GENIChomozygous54108865
7129503570129503571GA28GENIChomozygous54108866
7129503775129503776CT16GENIChomozygous54108867
7129503952129503953CT20GENIChomozygous54108868
7129504033129504034TC27GENIChomozygous54108869
7129504153129504154A-14GENIChomozygous54108870
7129504193129504194T-13GENIChomozygous54108871
7129504226129504227GT25GENIChomozygous54108872
7129504250129504251CA29GENIChomozygous54108873
7129504265129504266TTG27GENIChomozygous54108874
7129504713129504714CT29GENIChomozygous54108875
7129505002129505003CT30GENIChomozygous54108876
7129505220129505221CT24GENIChomozygous54108877
7129505485129505486GA33GENIChomozygous54108878
7129505772129505773TTC23GENIChomozygous54108879
7129506029129506030GA20GENIChomozygous54108880
7129506082129506083AG20GENIChomozygous54108881
7129506448129506449GA25GENIChomozygous54108882
7129507673129507674TC26GENIChomozygous54108883
7129508151129508153AT--38GENIChomozygous54108884