chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136508854136508855CT9GENIChomozygous56941166
4136509087136509088GA17GENIChomozygous56941167
4136509516136509517AG22GENIChomozygous56941168
4136510258136510259TA22GENIChomozygous56941169
4136513452136513453GA21GENIChomozygous56941170
4136514435136514436GA28GENICheterozygous56941171
4136514436136514437CT28GENICheterozygous56941172
4136514687136514688CT18GENIChomozygous56941173
4136515494136515495CT17GENICpossibly homozygous56941174
4136515686136515687GA21GENICpossibly homozygous56941175
4136515949136515953AGGT----11GENIChomozygous56941176
4136516602136516603TG8GENICpossibly homozygous56941177