chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62452762524527626TC75GENIChomozygous114743026
62452807924528080AG51GENIChomozygous114743027
62452818924528190GC71GENIChomozygous114743028
62452902324529024AG65GENIChomozygous114743029
62452923624529237GA48GENIChomozygous114743030
62452938024529381AG54GENIChomozygous114743031
62452960824529609TC57GENICpossibly homozygous114743032
62452966324529664AG60GENICpossibly homozygous114743033
62452980624529807CG40GENIChomozygous114743034
62453012724530128TC67GENIChomozygous114743035
62453016124530162TA53GENIChomozygous114743036
62453043624530437CT46GENICpossibly homozygous114743037
62453094424530945TC50GENIChomozygous114743038
62453117724531178TC64GENIChomozygous114743039
62453118724531188TC68GENIChomozygous114743040
62453221224532213AG60GENIChomozygous114743041