chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230272882230272883TG24GENICheterozygous74936691
2230273007230273008CG14GENICheterozygous74441326
2230273054230273055CT12GENICpossibly homozygous74936692
2230273081230273082GT16GENICheterozygous74936693
2230273441230273442AG5GENICheterozygous74936697
2230274721230274722CG10GENICheterozygous78717055
2230274800230274801AC17GENICheterozygous74936698
2230274897230274898CG9GENIChomozygous74936699
2230275373230275374AG8GENIChomozygous74936702
2230275469230275470GT24GENICpossibly homozygous74936703
2230275509230275510TC19GENIChomozygous74936704
2230275619230275620TC4GENICheterozygous74936705
2230275632230275633CG3GENIChomozygous78717056
2230275633230275634TC3GENIChomozygous78717057
2230275838230275839AG10GENIChomozygous74936707
2230276136230276137TA23GENIChomozygous74936708
2230276438230276439TC28GENIChomozygous74936709
2230276553230276554GC30GENIChomozygous74936710
2230276842230276843GA28GENIChomozygous74936711
2230277031230277032AG24GENIChomozygous74936712
2230277055230277056TC21GENIChomozygous74936713
2230277215230277216AG31GENIChomozygous74936714
2230277388230277389GT15GENIChomozygous74936716
2230277839230277840GC12GENIChomozygous74936717
2230278129230278130GT25GENIChomozygous74936718
2230275991230275992CA11GENICpossibly homozygous75571524