chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136508854136508855CT29GENIChomozygous56941166
4136509087136509088GA19GENIChomozygous56941167
4136509516136509517AG23GENIChomozygous56941168
4136510258136510259TA36GENIChomozygous56941169
4136513452136513453GA38GENIChomozygous56941170
4136514435136514436GA25GENIChomozygous56941171
4136514436136514437CT25GENIChomozygous56941172
4136514687136514688CT25GENIChomozygous56941173
4136515494136515495CT20GENIChomozygous56941174
4136515686136515687GA28GENICpossibly homozygous56941175
4136515949136515953AGGT----17GENIChomozygous56941176
4136516602136516603TG18GENIChomozygous56941177