chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135270529852705299CT26GENIChomozygous114550743
135270649052706491GA23GENIChomozygous114550744
135270694852706949AG19GENIChomozygous114550745
135270709352707094AT29GENICheterozygous114550746
135270852752708528GC24GENIChomozygous114550747
135271045552710456CT18GENIChomozygous114617574
135271101952711020GT20GENIChomozygous114550748
135271597052715971GA24GENIChomozygous114550749
135272713152727132CT28GENICpossibly homozygous114550751
135272748452727485GT25GENIChomozygous114550752
135273672552736726GA23GENIChomozygous114550753
135274263452742635AG39GENIChomozygous114550754