chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104522040945220410GT38GENIChomozygous116583225
104522095945220960CA34GENIChomozygous116583229
104522158645221587GC15GENIChomozygous116583231
104522435545224356TC21GENIChomozygous116583233
104522589045225891GA15GENIChomozygous116583235
104523367645233677CT17GENIChomozygous116583237
104523478945234790TC15GENIChomozygous116583241
104523963545239636AG17GENICpossibly homozygous116583243
104524007645240077AG19GENIChomozygous116583245
104524163545241636TC21GENIChomozygous116583247
104524231545242316TC30GENIChomozygous116583249