chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100476541100476542GA21GENIChomozygous978817804
4100476655100476656AG18GENIChomozygous978817805
4100477555100477556TC40GENIChomozygous978817806
4100477730100477731GA40GENIChomozygous978817807
4100478128100478129TC23GENIChomozygous978817808
4100480367100480368GA51GENIChomozygous978817809
4100480760100480761TC45GENIChomozygous978817810
4100482128100482129TC24GENIChomozygous978817811
4100482878100482879CA10GENIChomozygous978817812
4100483067100483068AG27GENIChomozygous978817813
4100483085100483086CT32GENIChomozygous978817814