chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129501912129501913GA15GENIChomozygous54108861
7129501942129501943AG14GENIChomozygous54108862
7129502043129502044TTCACACGCACA18GENIChomozygous54108863
7129502762129502763AG28GENIChomozygous54108864
7129503510129503511GT29GENIChomozygous54108865
7129503570129503571GA21GENIChomozygous54108866
7129503775129503776CT21GENIChomozygous54108867
7129503952129503953CT18GENIChomozygous54108868
7129504033129504034TC19GENIChomozygous54108869
7129504153129504154A-29GENIChomozygous54108870
7129504193129504194T-14GENIChomozygous54108871
7129504226129504227GT14GENIChomozygous54108872
7129504250129504251CA22GENIChomozygous54108873
7129504265129504266TTG28GENIChomozygous54108874
7129504713129504714CT26GENIChomozygous54108875
7129505002129505003CT15GENIChomozygous54108876
7129505220129505221CT20GENIChomozygous54108877
7129505485129505486GA38GENIChomozygous54108878
7129505772129505773TTC29GENIChomozygous54108879
7129506029129506030GA19GENIChomozygous54108880
7129506082129506083AG26GENIChomozygous54108881
7129506448129506449GA27GENIChomozygous54108882
7129507673129507674TC15GENIChomozygous54108883
7129508151129508153AT--28GENIChomozygous54108884