chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71194601111946012GT26GENIChomozygous53789772
71194614311946144CT6GENIChomozygous54558068
71194709411947095AT33GENIChomozygous53789773
71194747711947478CCAG26GENIChomozygous53789774
71194760911947610GA36GENIChomozygous53789775
71194795411947955CT31GENIChomozygous53789776
71194841811948419TC29GENIChomozygous53789777
71194937211949373AG33GENIChomozygous53789778
71194960911949610AG30GENIChomozygous53789779
71194968511949686CG31GENIChomozygous53789780
71194996211949963AG36GENIChomozygous53789781
71195027911950280AG31GENIChomozygous53789782
71195081611950817CT27GENIChomozygous53789783
71195100711951008AG26GENIChomozygous53789784
71195154111951542TC33GENIChomozygous53789785
71194618211946183GA9GENICpossibly homozygous54301718
71194618511946186TA9GENIChomozygous54301721
71194618811946189TC11GENIChomozygous54301724