chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8127906083127906084TA73GENIChomozygous117971713
8127906112127906113AG70GENIChomozygous116719728
8127906416127906417CT57GENIChomozygous117971714
8127909379127909380AG31GENIChomozygous116719730
8127910939127910940CG49GENICheterozygous116901144
8127914078127914079AG67GENIChomozygous116719780
8127909146127909146G48GENIChomozygous128646813
8127910565127910565C2GENIChomozygous128646814
8127913045127913046C51GENICpossibly homozygous128646815
8127909480127909481GT42GENICheterozygous128668476
8127909482127909483CG42GENICheterozygous128668477
8127909489127909490GA47GENICheterozygous128668478
8127910200127910201GA21GENIChomozygous128668479
8127910253127910254CT26GENIChomozygous128668480
8127909759127909760AG11GENICheterozygous133965512
8127909853127909854CT68GENICheterozygous132878028
8127910140127910141CT11GENICheterozygous117176076
8127914885127914886TA48GENIChomozygous117006850
8127913961127913962AG70GENIChomozygous116719738