chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5163247073163247074CT28GENIChomozygous55824665
5163247260163247261C-19GENIChomozygous55824667
5163247397163247398GA27GENIChomozygous55824669
5163247458163247459G-25GENIChomozygous55824671
5163247595163247602GCCAGCT-------19GENIChomozygous55824673
5163247708163247709TC27GENIChomozygous55824675
5163248330163248331TA15GENIChomozygous55824677
5163248352163248353GA12GENIChomozygous55824679
5163248833163248834TA21GENIChomozygous55824681
5163249096163249097TC24GENIChomozygous55824683
5163249281163249286TTTTC-----13GENICheterozygous55824685
5163250304163250305GA24GENIChomozygous55824687
5163250314163250315A-20GENIChomozygous55824689
5163250673163250674GA19GENIChomozygous55824691
5163250696163250697TG15GENIChomozygous55824693
5163250729163250730TC17GENIChomozygous55824695
5163250995163250996AG18GENIChomozygous55824697
5163251936163251937C-48GENICheterozygous56192879