chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101318932113189322AT69GENICpossibly homozygous142217016
101319007113190072CT67GENIChomozygous142217017
101319232113192322TC46GENIChomozygous142217018
101319268513192686GC63GENIChomozygous142217019
101319305213193053GA46GENIChomozygous138725729
101319339413193396CG48GENIChomozygous142196596
101319396613193967GT55GENIChomozygous138725730
101319339513193396G48GENIChomozygous403276747
101319339513193396GA48GENICheterozygous154678249