chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140565949140565950GA4GENIChomozygous113057112
4140567416140567417TA16GENIChomozygous113057116
4140567719140567720GA23GENIChomozygous113057118
4140568687140568688CT16GENIChomozygous113057120
4140568993140568994AG25GENIChomozygous113057122
4140569239140569240AT18GENIChomozygous113057124
4140569525140569526GA5GENICheterozygous126118801
4140570080140570081TG7GENIChomozygous113057126
4140570084140570085AG9GENIChomozygous112857632
4140572950140572951AG22GENIChomozygous113057128
4140573002140573003AG18GENIChomozygous113057130
4140573909140573910GC20GENIChomozygous113057132
4140573928140573929CT17GENIChomozygous113057134
4140574076140574077AG9GENIChomozygous113057136
4140574078140574079GA10GENIChomozygous113057138
4140574155140574156CG5GENIChomozygous113562518
4140574548140574549GA9GENIChomozygous113057142
4140574608140574609CT14GENIChomozygous113057144
4140574770140574771AG14GENIChomozygous113057146
4140575255140575256GA22GENIChomozygous113057148
4140575893140575894TG19GENIChomozygous112857642
4140578417140578418GA16GENIChomozygous113057150
4140593585140593586CA20GENIChomozygous112857694
4140593636140593637AT10GENIChomozygous113057152
4140593642140593643CT13GENIChomozygous112857696