chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136508854136508855CT53GENICpossibly homozygous56941166
4136509087136509088GA40GENIChomozygous56941167
4136509516136509517AG62GENIChomozygous56941168
4136510258136510259TA63GENIChomozygous56941169
4136513452136513453GA50GENIChomozygous56941170
4136514435136514436GA46GENIChomozygous56941171
4136514436136514437CT47GENIChomozygous56941172
4136514687136514688CT44GENIChomozygous56941173
4136515494136515495CT49GENIChomozygous56941174
4136515686136515687GA44GENIChomozygous56941175
4136515949136515953AGGT----52GENIChomozygous56941176
4136516602136516603TG23GENIChomozygous56941177