chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148252903482529035TC52GENIChomozygous66542717
148253417782534178GT53GENIChomozygous66983710
148254457682544577AC23GENICpossibly homozygous66983714
148254732982547330CT69GENIChomozygous66983716
148255287182552872GA55GENICpossibly homozygous66983718
148255468982554690AG54GENIChomozygous66542726
148255739382557394GA57GENICpossibly homozygous66645913
148256141982561420AC39GENIChomozygous66542730
148256291982562920TC54GENICpossibly homozygous66542731
148256309482563095TC60GENIChomozygous66542732
148256389082563891AT88GENICheterozygous66542733
148256763982567640GA56GENIChomozygous66542735
148256793982567940AG116GENICheterozygous66105699
148256784082567841CT79GENICheterozygous66105693
148256784582567846TC79GENICheterozygous66105695
148256790982567910CA118GENICheterozygous66105697
148256795982567960AG101GENICheterozygous66105701
148256799982568000TC64GENICheterozygous66105703
148256801182568012CT60GENICheterozygous66105705
148257182382571824GA52GENIChomozygous66983720
148257270782572708GA55GENIChomozygous66983722
148257483282574833AG55GENIChomozygous66542740
148257955682579557AG56GENICpossibly homozygous66983724
148257986682579867CA45GENIChomozygous66983726