chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230272882230272883TG28GENIChomozygous74936691
2230274897230274898CG8GENIChomozygous74936699
2230275083230275084AC8GENICpossibly homozygous74936700
2230275322230275323TG10GENICpossibly homozygous74936701
2230275373230275374AG8GENIChomozygous74936702
2230275469230275470GT11GENIChomozygous74936703
2230275509230275510TC7GENIChomozygous74936704
2230276136230276137TA21GENIChomozygous74936708
2230276438230276439TC31GENIChomozygous74936709
2230276553230276554GC27GENIChomozygous74936710
2230276842230276843GA33GENICpossibly homozygous74936711
2230277031230277032AG29GENIChomozygous74936712
2230277055230277056TC27GENIChomozygous74936713
2230277215230277216AG26GENIChomozygous74936714
2230277388230277389GT29GENIChomozygous74936716
2230277839230277840GC13GENIChomozygous74936717
2230278129230278130GT29GENIChomozygous74936718
2230275991230275992CA11GENICheterozygous75571524