chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146262850962628510AG63GENIChomozygous113479123
146262878962628790AG57GENIChomozygous113479124
146262888462628885AT63GENIChomozygous113479125
146262893662628937T52GENICpossibly homozygous129166892
146262925362629253TGGC44GENIChomozygous129166893
146263000262630003TC56GENIChomozygous113479126
146263127262631273TC53GENIChomozygous113479127
146263150362631504GA60GENIChomozygous113479128
146263155762631558AT65GENIChomozygous113479129
146263161862631618A66GENIChomozygous129166894
146263183962631840TA63GENIChomozygous113479130
146263196662631967C59GENIChomozygous129166895
146263232462632325TC57GENIChomozygous113479131
146263261662632617CT60GENIChomozygous113479132
146263265862632659CA68GENIChomozygous113479133
146263283962632840GC63GENIChomozygous113479134
146263323062633231GT55GENIChomozygous113479135
146263367262633673CG50GENIChomozygous113479136
146263411662634118AC40GENICpossibly homozygous129166896
146263442762634427A47GENIChomozygous129166897
146263462862634629TC48GENIChomozygous113479137
146263532462635325AG61GENIChomozygous113479138
146263532662635331GAATG60GENIChomozygous129166898
146263533362635333GTCG61GENIChomozygous129166899
146263591462635915CT43GENIChomozygous113479139
146263764962637650TC49GENIChomozygous113479140
146263821662638217GA56GENIChomozygous113479141
146263891662638917GA53GENIChomozygous113479142
146263453462634535CT34GENIChomozygous113678003
146263979762639797A59GENICpossibly homozygous129166900
146264128462641285TA54GENIChomozygous113479143
146264148162641481A48GENICpossibly homozygous129166901
146264302962643030TC58GENIChomozygous113479144
146264317962643180AG52GENIChomozygous113479145
146264354562643546AG51GENIChomozygous113479146
146264415162644152CT45GENIChomozygous113479147
146264544062645441CG65GENIChomozygous113479148
146264560362645604AG50GENIChomozygous113479149