chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31457366714573668G1GENIChomozygous129887711
31457367814573679C4GENIChomozygous129887712
31457368714573687G8GENIChomozygous129887713
31457368914573691CC9GENIChomozygous129887714
31457369814573699CG10GENIChomozygous129894048
31457370314573704C11GENIChomozygous129887715
31457370514573706A12GENIChomozygous129887716
31457371614573717A14GENIChomozygous129887717
31457372214573723TG15GENIChomozygous129894049
31457372714573728C15GENIChomozygous129887718
31457373114573733CA17GENIChomozygous129887719
31457373414573734T17GENIChomozygous129887720
31457392914573930CT28GENIChomozygous112407501
31457418414574185GA33GENIChomozygous112407504
31457435714574358TA62GENIChomozygous111880010
31457440314574404AG72GENIChomozygous111880012
31457442514574426AG67GENIChomozygous111880014
31457452314574524AG49GENIChomozygous111453432
31457453414574535GA46GENIChomozygous112407506
31457463014574631TG45GENIChomozygous111880018
31457469214574693CG41GENIChomozygous112407508
31457470414574705CT41GENIChomozygous111880020
31457481114574812AC56GENICpossibly homozygous111880022
31457499814574999CT45GENIChomozygous111880032
31457483514574836TC55GENICpossibly homozygous111880024
31457483614574837TC54GENICpossibly homozygous111880026
31457486814574869CT57GENICpossibly homozygous111880028
31457492614574927CA52GENICpossibly homozygous111880030
31457483914574842TGA53GENICpossibly homozygous132038870
31457510714575108CT32GENIChomozygous112407510
31457523114575232AT28GENICpossibly homozygous111880034
31457525514575256GA26GENICpossibly homozygous112407512
31457525714575258GA26GENICpossibly homozygous112407514
31457531214575313CA29GENIChomozygous111880036
31457534814575349AT28GENIChomozygous111880038