chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT55GENIChomozygous507632929
10108877194108877195CT57GENIChomozygous507632930
10108877595108877596TG53GENIChomozygous507632931
10108877657108877658AG50GENIChomozygous507632932
10108877811108877812GA29GENICheterozygous510624475
10108877841108877842CT21GENICheterozygous510624476
10108877927108877928CT13GENICheterozygous507632933
10108878538108878539CCTT9GENIChomozygous686161261
10108878562108878563CCTT11GENICpossibly homozygous686161263
10108878644108878645TC38GENICpossibly homozygous507632934