chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106072498106072499AG61GENIChomozygous144875971
10106073150106073151GC65GENIChomozygous144875972
10106073723106073724AG58GENIChomozygous144875973
10106074463106074464CT78GENIChomozygous144875974
10106075519106075520TC60GENIChomozygous144875975
10106075580106075581TC70GENICpossibly homozygous144875976
10106077106106077107CT55GENIChomozygous144875977
10106077546106077547GC61GENIChomozygous138868395
10106082171106082172AG71GENIChomozygous144875978
10106083680106083681CT68GENIChomozygous144875979
10106089203106089204G64GENIChomozygous138703563