chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1124829373124829374CT22GENICpossibly homozygous120670038
1124834348124834349CT39GENIChomozygous108924450
1124834587124834588GA28GENIChomozygous108924451
1124834664124834665TG20GENIChomozygous108924452
1124835416124835417CT20GENIChomozygous108924453
1124835446124835447AG19GENIChomozygous108924454
1124835917124835918AG21GENIChomozygous108924455