chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115473973115473974GA52GENIChomozygous112815704
4115475057115475058TC66GENICheterozygous112815706
4115476171115476172TC46GENIChomozygous112815708
4115476442115476443GA54GENIChomozygous112815710
4115476474115476475TA58GENIChomozygous112815712
4115476501115476502GA65GENIChomozygous112815714
4115476722115476723AG42GENIChomozygous112815716
4115477341115477342AG64GENICpossibly homozygous112815718
4115478351115478352TG85GENIChomozygous112815720
4115478489115478490AG69GENIChomozygous112815722
4115479171115479172TC55GENIChomozygous112815724
4115480465115480466AG61GENIChomozygous112815726
4115481701115481702CT42GENIChomozygous112815728
4115481866115481867CG54GENIChomozygous112815730
4115481873115481874GA60GENIChomozygous112815732
4115483110115483111TC62GENICpossibly homozygous112815734
4115483945115483946TC51GENIChomozygous112815736
4115484515115484516GA67GENIChomozygous112815738