chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121297735121297736AG39GENIChomozygous115858312
7121298423121298424AG40GENIChomozygous115858314
7121298431121298432GC36GENIChomozygous115858316
7121298452121298453CT30GENIChomozygous115858318
7121298492121298493TC35GENIChomozygous115858320
7121298664121298665AG25GENIChomozygous115858322
7121299164121299165CT29GENIChomozygous115858324
7121299573121299574AG37GENIChomozygous115858326
7121299607121299608AG35GENIChomozygous115858328
7121299782121299783TC35GENIChomozygous115858330
7121299980121299981TC31GENIChomozygous115858332
7121300244121300245TG31GENIChomozygous115858334
7121300507121300508CG38GENIChomozygous115858336
7121301550121301551GA33GENICpossibly homozygous115858338
7121301976121301977CG29GENIChomozygous115858340
7121302002121302003GT29GENIChomozygous115858342
7121302007121302008CG28GENIChomozygous115858344
7121302030121302031CA19GENIChomozygous115858346