chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136508854136508855CT6GENICheterozygous56941166
4136509087136509088GA10GENICpossibly homozygous56941167
4136509516136509517AG14GENICpossibly homozygous56941168
4136510258136510259TA8GENIChomozygous56941169
4136513452136513453GA19GENIChomozygous56941170
4136514435136514436GA12GENICheterozygous56941171
4136514436136514437CT12GENICheterozygous56941172
4136514687136514688CT21GENICpossibly homozygous56941173
4136515494136515495CT9GENICheterozygous56941174
4136515686136515687GA16GENIChomozygous56941175
4136515949136515953AGGT----12GENIChomozygous56941176
4136516602136516603TG4GENICheterozygous56941177