chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230272882230272883TG13GENICheterozygous74936691
2230273007230273008CG7GENICheterozygous74441326
2230273054230273055CT3GENIChomozygous74936692
2230273081230273082GT4GENICheterozygous74936693
2230274800230274801AC6GENICheterozygous74936698
2230274897230274898CG13GENIChomozygous74936699
2230275322230275323TG15GENICheterozygous74936701
2230275373230275374AG10GENIChomozygous74936702
2230275469230275470GT14GENIChomozygous74936703
2230275509230275510TC14GENIChomozygous74936704
2230275602230275603AG3GENIChomozygous74441330
2230275838230275839AG19GENICheterozygous74936707
2230276136230276137TA23GENIChomozygous74936708
2230276438230276439TC15GENIChomozygous74936709
2230276553230276554GC20GENIChomozygous74936710
2230276842230276843GA12GENICpossibly homozygous74936711
2230277031230277032AG13GENIChomozygous74936712
2230277055230277056TC10GENIChomozygous74936713
2230277215230277216AG21GENIChomozygous74936714
2230277388230277389GT12GENIChomozygous74936716
2230277839230277840GC24GENIChomozygous74936717
2230278129230278130GT20GENIChomozygous74936718
2230275632230275633CG5GENIChomozygous78717056
2230275991230275992CA19GENIChomozygous75571524