chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228338247228338248CT53GENIChomozygous109000583
1228338307228338308AT49GENIChomozygous109000584
1228338817228338818CT40GENIChomozygous109000585
1228338840228338841AG42GENIChomozygous120596488
1228338921228338922GA39GENIChomozygous109000586
1228339573228339574GT32GENIChomozygous109000587
1228339707228339708GC38GENIChomozygous109000588
1228341518228341519TG42GENIChomozygous120596490
1228341875228341875C14GENIChomozygous130834034
1228341948228341949TC26GENIChomozygous120596492
1228341987228341988GA36GENIChomozygous120596494
1228342004228342005TC37GENIChomozygous109000590
1228342444228342445CG29GENIChomozygous109000591
1228342592228342592C26GENIChomozygous132539314
1228342595228342595G26GENIChomozygous132539315
1228342620228342621GC24GENIChomozygous132556954
1228345224228345225CT31GENIChomozygous109000598
1228345365228345366GA40GENIChomozygous120596496
1228347641228347642AC41GENIChomozygous109000602
1228348065228348066AG55GENIChomozygous120491642
1228348066228348067GC55GENIChomozygous120491643
1228353262228353263CA51GENIChomozygous120596498
1228353448228353449AT36GENIChomozygous109000613
1228357580228357581CT41GENIChomozygous109000618
1228359321228359323AG50GENIChomozygous133054384
1228359736228359737AG51GENIChomozygous109000627
1228368316228368317TC45GENIChomozygous120596502
1228369099228369100CG44GENIChomozygous109000642
1228342628228342631TTT23GENIChomozygous134780546
1228342658228342659G28GENIChomozygous134780547
1228345932228345933GC22GENICheterozygous130853778