chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140564983140564984GA47GENICpossibly homozygous112857626
4140565941140565942GA47GENICheterozygous113057110
4140565949140565950GA47GENICheterozygous113057112
4140567416140567417TA40GENIChomozygous113057116
4140567719140567720GA48GENIChomozygous113057118
4140568687140568688CT29GENIChomozygous113057120
4140568993140568994AG66GENIChomozygous113057122
4140569239140569240AT28GENIChomozygous113057124
4140570080140570081TG31GENIChomozygous113057126
4140570084140570085AG31GENIChomozygous112857632
4140572950140572951AG29GENIChomozygous113057128
4140573002140573003AG46GENIChomozygous113057130
4140573909140573910GC36GENIChomozygous113057132
4140573928140573929CT40GENIChomozygous113057134
4140574076140574077AG34GENIChomozygous113057136
4140574078140574079GA35GENIChomozygous113057138
4140574272140574273CT26GENICpossibly homozygous113057140
4140574548140574549GA44GENIChomozygous113057142
4140574608140574609CT41GENIChomozygous113057144
4140574770140574771AG49GENIChomozygous113057146
4140575255140575256GA56GENIChomozygous113057148
4140575893140575894TG33GENIChomozygous112857642
4140576235140576236TA45GENIChomozygous112857644
4140578417140578418GA45GENIChomozygous113057150
4140593585140593586CA65GENICpossibly homozygous112857694
4140593636140593637AT53GENIChomozygous113057152
4140593642140593643CT49GENIChomozygous112857696