chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2049181124918113TC69GENICheterozygous109490624
2049203044920305AC23GENIChomozygous109233694
2049204994920500GA17GENIChomozygous109075658
2049205084920509GA18GENIChomozygous109075660
2049206074920608CA14GENIChomozygous109075662
2049206314920632CT11GENIChomozygous109075664
2049206574920658AC8GENIChomozygous109075667
2049207614920762TA16GENIChomozygous109075669
2049213494921350CG9GENIChomozygous109296469
2049213564921357TG9GENIChomozygous109296471
2049213664921367GA10GENIChomozygous109296473
2049213774921378CT9GENIChomozygous109296475
2049213824921383AT10GENIChomozygous109477799
2049216724921673AG20GENIChomozygous109075671
2049212404921241TC3GENIChomozygous109506045
2049215074921508AG17GENIChomozygous109506048