chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
499370719937072AG59GENIChomozygous112492995
499370759937076TC59GENIChomozygous112492997
499372749937275GA67GENIChomozygous112492999
499372869937287CT67GENIChomozygous112493001
499372989937299GA72GENICpossibly homozygous112493003
499373219937322GA69GENIChomozygous112493005
499373999937400GA69GENIChomozygous112493007
499374609937461CA74GENIChomozygous112493009
499375489937549CT81GENIChomozygous112493011
499376549937655TG52GENIChomozygous112493013
499377019937702GA59GENIChomozygous112493015
499377219937722GA58GENIChomozygous112493016
499377349937735AC59GENIChomozygous112493018
499377469937747AG56GENIChomozygous112493020
499379589937959GT73GENIChomozygous112493022
499380479938048CG60GENIChomozygous112493024
499381759938176AG58GENIChomozygous112493026
499382179938218TA78GENIChomozygous112493028
499382519938252TA85GENICpossibly homozygous112493030
499384169938417CG57GENIChomozygous112493032
499384349938435GT52GENIChomozygous112493034
499384509938451TC52GENIChomozygous112493036
499384829938483GT59GENIChomozygous112493038
499388009938801GT69GENIChomozygous112493040
499388499938850CT57GENIChomozygous112493042
499388799938880AG55GENIChomozygous112493044
499388879938888GC52GENIChomozygous112493046