chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106340944363409444GA73GENIChomozygous142254212
106340959463409595AG71GENIChomozygous138804699
106341035663410357CT43GENIChomozygous142254213
106341039363410393G55GENIChomozygous142204941
106341065063410651GA37GENIChomozygous142254214
106341111263411113AG50GENICpossibly homozygous142254215
106341180663411807CT40GENIChomozygous142254216
106341341763413418TC66GENIChomozygous138804709
106341391563413916CT59GENIChomozygous138804710
106341398863413988T55GENIChomozygous142204942
106341509463415099TTGAT61GENIChomozygous142204943
106341642263416423TC42GENIChomozygous138804719
106341732763417328AG67GENIChomozygous138804722