chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4169766380169766381AG39GENIChomozygous137265566
4169767644169767645CT46GENIChomozygous137265567
4169767745169767746CT52GENIChomozygous143168556
4169767788169767789CT52GENIChomozygous137265568
4169767986169767987TC37GENIChomozygous137265569
4169768648169768649GA43GENIChomozygous137265570
4169768789169768790GA47GENIChomozygous137265571
4169769519169769520GA46GENIChomozygous137265572