chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161263024161263025GT39GENIChomozygous798071250
3161263208161263209TC26GENIChomozygous798071251
3161264132161264133AG36GENIChomozygous798071252
3161264323161264324GA27GENIChomozygous798071253
3161265050161265051CA15GENIChomozygous798071254
3161266300161266301GT19GENICpossibly homozygous798071255
3161269826161269827GA46GENIChomozygous798071256
3161270225161270226TC33GENIChomozygous798071257