chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142185333142185334CT18GENIChomozygous108937405
1142185583142185584CG28GENIChomozygous108937406
1142186364142186365GA17GENIChomozygous108937407
1142187798142187799GA27GENIChomozygous108937408
1142190388142190389GT31GENIChomozygous108262834
1142188814142188815AG32GENIChomozygous108262828
1142190034142190035AG19GENIChomozygous108262832
1142191294142191295GA15GENIChomozygous108262838
1142191311142191312AG13GENIChomozygous108262840
1142191427142191428AG22GENIChomozygous108937409
1142193164142193165CT17GENIChomozygous108937410
1142193608142193609CT29GENIChomozygous108937411
1142196376142196377AG26GENIChomozygous108262844
1142197535142197536TC9GENIChomozygous108262846