chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185548379955483800TC4GENIChomozygous125390645
185548740855487409GA5GENICheterozygous125352249
185548769455487695GT7GENICheterozygous125390646
185548818655488187AG7GENIChomozygous125352251
185549489555494896GA4GENIChomozygous119547729
185549658355496584AG8GENIChomozygous110359975
185549716055497161CT21GENICheterozygous119494967
185549718955497190TC8GENICheterozygous119494968
185549719355497194TC7GENICheterozygous119494969
185549924555499246CG9GENICheterozygous119532860
185549932855499329GA20GENICheterozygous119532862
185549980355499804TA8GENIChomozygous125352259
185549990255499903GT5GENIChomozygous125414114
185549662655496627GC14GENICheterozygous125414110
185549927655499277TC19GENICheterozygous125414111
185549978655499787AC5GENIChomozygous125414112
185549983355499834TC4GENICheterozygous125414113
185549671855496719GA12GENIChomozygous110592551
185549999155499992CT8GENICheterozygous125414115
185550000755500008CT7GENIChomozygous125414116
185550025055500251CA14GENICheterozygous125414117
185550043355500434AC34GENIChomozygous125352263
185550068855500689CT5GENICheterozygous125414118
185550155555501556GT15GENIChomozygous125414119
185550158455501585AG22GENICpossibly homozygous125414120
185550159055501591GA18GENIChomozygous125414121
185550159155501592GA17GENICheterozygous125414122
185550177355501774CT6GENICheterozygous125390650
185550376455503765TC12GENIChomozygous125352273
185550456455504565GA21GENICheterozygous125414123