chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230272882230272883TG29GENICheterozygous74936691
2230273007230273008CG22GENICheterozygous74441326
2230273054230273055CT5GENICheterozygous74936692
2230273181230273182GC7GENIChomozygous74936694
2230275322230275323TG12GENICheterozygous74936701
2230275469230275470GT17GENIChomozygous74936703
2230275602230275603AG5GENIChomozygous74441330
2230275619230275620TC3GENIChomozygous74936705
2230275632230275633CG3GENICheterozygous78717056
2230275633230275634TC3GENICheterozygous78717057
2230275838230275839AG9GENICpossibly homozygous74936707
2230276136230276137TA31GENIChomozygous74936708
2230276438230276439TC28GENIChomozygous74936709
2230276553230276554GC40GENIChomozygous74936710
2230276842230276843GA22GENIChomozygous74936711
2230277031230277032AG19GENIChomozygous74936712
2230277055230277056TC26GENIChomozygous74936713
2230277215230277216AG15GENIChomozygous74936714
2230277388230277389GT15GENIChomozygous74936716
2230277839230277840GC21GENIChomozygous74936717
2230278129230278130GT23GENIChomozygous74936718
2230275991230275992CA14GENIChomozygous75571524