chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127906083127906084TA26GENIChomozygous117971713
8127906112127906113AG25GENIChomozygous116719728
8127906416127906417CT21GENIChomozygous117971714
8127909379127909380AG16GENIChomozygous116719730
8127909853127909854CT23GENICheterozygous132878028
8127910939127910940CG18GENICheterozygous116901144
8127913961127913962AG20GENIChomozygous116719738
8127914078127914079AG18GENIChomozygous116719780
8127909146127909146G17GENIChomozygous128646813
8127910565127910565C6GENIChomozygous128646814
8127913045127913046C18GENIChomozygous128646815
8127909480127909481GT14GENICpossibly homozygous128668476
8127909482127909483CG14GENICpossibly homozygous128668477
8127909489127909490GA13GENICpossibly homozygous128668478
8127910200127910201GA9GENIChomozygous128668479
8127910253127910254CT14GENIChomozygous128668480
8127914885127914886TA18GENIChomozygous117006850