chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1209464082209464083GGT3GENICheterozygous62274944
1209464286209464288CA--18GENICheterozygous62274945
1209467854209467856AC--10GENICheterozygous62274947
1209475932209475933G-7GENICheterozygous61071421
1209488328209488331TTA---10GENICheterozygous62413394
1209489835209489836AATG15GENIChomozygous61071502
1209490272209490273T-5GENICheterozygous61071505
1209493297209493298GT8GENIChomozygous61071522
1209503972209503973AATATC8GENIChomozygous62470386
1209512622209512625GAT---14GENICheterozygous62413396
1209528723209528725TA--11GENICheterozygous62274950
1209546907209546914CAGAGCA-------24GENIChomozygous61071727
1209546965209546966AC24GENIChomozygous61071730
1209546966209546967CA23GENIChomozygous61071731
1209547003209547004C-21GENIChomozygous61071732
1209547071209547072C-24GENIChomozygous61071734
1209549558209549559TTCC33GENIChomozygous61071742
1209550994209550995GGTCTC4GENIChomozygous62344330
1209555516209555517C-15GENIChomozygous61071758
1209555524209555525C-13GENIChomozygous61071759
1209555536209555537TA17GENIChomozygous62194531
1209555537209555538AG17GENIChomozygous62194533
1209555543209555544G-19GENIChomozygous61071760
1209555552209555553AAG18GENIChomozygous61071761
1209555755209555756CCA19GENIChomozygous61071763
1209555757209555758CCA19GENIChomozygous61071764
1209560887209560889TT--10GENICheterozygous61071785
1209560888209560889T-10GENICheterozygous61071786
1209567613209567615CA--8GENICheterozygous62248672