chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190556105190556106GT31GENIChomozygous108465670
1190565529190565530CT23GENIChomozygous108977837
1190567366190567367GC28GENIChomozygous108465679
1190574019190574020AG30GENIChomozygous108465687
1190574020190574021AG30GENIChomozygous108465688
1190579108190579109AC26GENIChomozygous108465697
1190582481190582482CT29GENICpossibly homozygous108977838