chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140564983140564984GA45GENIChomozygous112857626
4140565940140565941G46GENIChomozygous130938170
4140565943140565950AGGAAGG46GENIChomozygous130938171
4140566231140566231AT20GENIChomozygous130938172
4140567416140567417TA59GENIChomozygous113057116
4140567719140567720GA62GENIChomozygous113057118
4140568687140568688CT47GENIChomozygous113057120
4140568993140568994AG54GENIChomozygous113057122
4140569239140569240AT49GENIChomozygous113057124
4140569512140569526CACACACACACACG51GENICheterozygous130938173
4140570080140570081TG75GENIChomozygous113057126
4140570084140570085AG72GENIChomozygous112857632
4140572950140572951AG65GENIChomozygous113057128
4140573002140573003AG70GENIChomozygous113057130
4140573909140573910GC55GENIChomozygous113057132
4140573928140573929CT57GENIChomozygous113057134
4140574076140574077AG48GENIChomozygous113057136
4140574078140574079GA46GENIChomozygous113057138
4140574152140574152TG29GENICheterozygous130938174
4140574272140574273CT10GENIChomozygous113057140
4140574365140574366T26GENIChomozygous130938175
4140574509140574510T47GENIChomozygous130938176
4140574548140574549GA56GENIChomozygous113057142
4140574608140574609CT47GENIChomozygous113057144
4140574633140574634A52GENIChomozygous130938177
4140574770140574771AG34GENIChomozygous113057146
4140575255140575256GA57GENIChomozygous113057148
4140575893140575894TG46GENIChomozygous112857642
4140576235140576236TA16GENIChomozygous112857644
4140578417140578418GA6GENIChomozygous113057150
4140575875140575876A44GENIChomozygous128085083
4140587419140587420C3GENIChomozygous130546969
4140593585140593586CA66GENICpossibly homozygous112857694
4140593636140593637AT62GENIChomozygous113057152
4140593642140593643CT61GENIChomozygous112857696