chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75040372950403730CT9GENICheterozygous54385494
75040933350409334GA11GENIChomozygous54650501
75040939650409397GGA2GENIChomozygous53917077
75040966250409663TC12GENICpossibly homozygous53917080
75041047750410478GC13GENICpossibly homozygous53917090
75041056850410569TC12GENICpossibly homozygous53917091
75041067750410678GA13GENIChomozygous53917092
75041072350410725TT--4GENIChomozygous54385496
75041074450410745GT8GENICpossibly homozygous53917094
75041145550411456CA11GENICpossibly homozygous53917095
75041157850411579CT9GENICpossibly homozygous53917096
75041205250412053AG13GENIChomozygous53917097
75041214650412147TG11GENICpossibly homozygous53917098
75041216250412163CT16GENICpossibly homozygous53917099
75041252150412522GGTT6GENIChomozygous54385502
75041258450412585CT11GENICpossibly homozygous53917101
75041275550412756AG12GENIChomozygous53917103
75041330650413307TC16GENIChomozygous53917104
75041344150413442TC15GENICpossibly homozygous53917105
75041467850414679TC12GENICpossibly homozygous53917107
75041498850414989GA11GENIChomozygous53917108
75041512350415124TC2GENIChomozygous53917109
75041525250415253GT10GENIChomozygous53917110
75041533650415337CT10GENIChomozygous53917111
75041540250415403AG9GENIChomozygous53917112
75041549350415494CT15GENIChomozygous53917113
75041551350415514TC14GENIChomozygous53917114
75041601550416016AG19GENIChomozygous53917115
75041628650416287GA7GENIChomozygous53917116
75041713050417131CT15GENIChomozygous53917120
75041770350417704C-15GENIChomozygous53917121
75041798050417981TG8GENIChomozygous53917122
75041925550419256AG6GENIChomozygous53917124
75041930050419301GC5GENIChomozygous53917125
75041950250419503TC9GENIChomozygous53917126
75041951050419511AT9GENIChomozygous53917127
75041973850419739TC6GENIChomozygous53917128
75041974350419744AG7GENIChomozygous53917129
75042012050420121TC16GENICpossibly homozygous53917130
75042038550420386TC9GENIChomozygous53917131
75041346850413469T-7GENICheterozygous54571817