chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2067590206759021GA13INTERGENIChomozygous63644178
2067594516759452GT14INTERGENIChomozygous63644179
2067595526759553CT21INTERGENIChomozygous63347436
2067604196760420CG17INTERGENIChomozygous63644180
2067609316760932AG22INTERGENIChomozygous63347442
2067620526762053TC29INTERGENIChomozygous63347446
2067635656763566CA7INTERGENIChomozygous63644181
2067646276764628GA5INTERGENIChomozygous63347454
2067646896764690CA15INTERGENIChomozygous63644182
2067647176764718CG10INTERGENIChomozygous63347458
2067654936765494CT12INTERGENIChomozygous63644184
2067656516765652GA24INTERGENICpossibly homozygous63644185
2067686726768673AG13INTERGENIChomozygous63347469
2067692226769223CT15INTERGENIChomozygous63644187
2067707546770755AG15GENIChomozygous63347475
2067715996771600GA22GENIChomozygous63644188
2067716116771612TC22GENIChomozygous63644189
2067716186771619GA18GENIChomozygous63644190
2067718666771867CT2GENIChomozygous84980881
2067718626771863CT2GENIChomozygous84980874
2067718636771864CT2GENIChomozygous84980876
2067718646771865CT2GENIChomozygous84980878
2067718656771866CT2GENIChomozygous84980879
2067718676771868CT2GENIChomozygous84980882
2067723386772339TC16GENIChomozygous63644192
2067724006772401CG21GENIChomozygous63347479
2067724376772438CA17GENIChomozygous63644193
2067724696772470AG16GENIChomozygous63644194
2067726556772656TG14GENIChomozygous63644195
2067733986773399TG6GENIChomozygous63644197
2067753156775316AG21GENICpossibly homozygous63644198
2067759976775998TC18GENICpossibly homozygous63644199
2067764906776491CT25GENIChomozygous63644200
2067769436776944TA23GENIChomozygous63644201
2067780706778071GA31GENIChomozygous63347483
2067781386778139CT23GENIChomozygous63644203
2067786806778681CT13GENIChomozygous63644204