chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
499370719937072AG30GENIChomozygous112492995
499370759937076TC30GENIChomozygous112492997
499372749937275GA13GENIChomozygous112492999
499372869937287CT13GENIChomozygous112493001
499372989937299GA15GENIChomozygous112493003
499373219937322GA13GENIChomozygous112493005
499373999937400GA20GENIChomozygous112493007
499374609937461CA26GENIChomozygous112493009
499375489937549CT32GENIChomozygous112493011
499376549937655TG21GENIChomozygous112493013
499377019937702GA15GENIChomozygous112493015
499377219937722GA17GENIChomozygous112493016
499377349937735AC17GENIChomozygous112493018
499377469937747AG15GENIChomozygous112493020
499379589937959GT21GENIChomozygous112493022
499380479938048CG32GENIChomozygous112493024
499381759938176AG32GENIChomozygous112493026
499382179938218TA32GENIChomozygous112493028
499382519938252TA35GENIChomozygous112493030
499384169938417CG25GENIChomozygous112493032
499384349938435GT30GENIChomozygous112493034
499384509938451TC31GENIChomozygous112493036
499384829938483GT36GENIChomozygous112493038
499388009938801GT25GENIChomozygous112493040
499388499938850CT39GENIChomozygous112493042
499388799938880AG39GENIChomozygous112493044
499388879938888GC42GENIChomozygous112493046