chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151620881151620882GT5GENICheterozygous125914150
3151622356151622357TC10GENIChomozygous125839890
3151622879151622880CA12GENIChomozygous125839891
3151623159151623160TC12GENIChomozygous125839892
3151623773151623774AG11GENIChomozygous125839893
3151624416151624417CG12GENIChomozygous125896150
3151625157151625158AG19GENIChomozygous125839894
3151629303151629304GA17GENIChomozygous125896152
3151629878151629879GT18GENIChomozygous125839898
3151631123151631124CT9GENIChomozygous125896153
3151635789151635790GA17GENIChomozygous125839903
3151637235151637236GT6GENICheterozygous125869426
3151639191151639192GA17GENIChomozygous125896154
3151640339151640340GA19GENIChomozygous125914154
3151641020151641021TC18GENIChomozygous125896155
3151641924151641925TC20GENIChomozygous125839908
3151645376151645377GT3GENICheterozygous125965271