chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104465345444653455TC22GENIChomozygous138782908
104465448844654489GA17GENIChomozygous138782909
104465614944656150TC24GENIChomozygous138782910
104465619644656197TC27GENIChomozygous138782911
104465809344658094TC22GENIChomozygous138782912
104465586644655867G28GENIChomozygous138681864
104465796044657960CA19GENIChomozygous138681865
104465892444658924GT11GENIChomozygous138681866
104466437944664380G30GENIChomozygous138681868
104466632744666328CT22GENIChomozygous138782916
104465891644658917GA13GENICheterozygous154632116
104465891644658917GT13GENIChomozygous154632117
104466296944662970AG19GENIChomozygous154632120
104466437944664380GA30GENICheterozygous154632121
104466085844660859AC22GENICpossibly homozygous138782913
104466123244661233AG28GENIChomozygous138782914
104466409744664098AG18GENIChomozygous138782915
104466296944662970A19GENICheterozygous403285227
104466662944666630AG20GENIChomozygous138782917
104466809844668099GT16GENIChomozygous138782918
104466810744668108CT15GENIChomozygous138782919
104466866644668667TA18GENIChomozygous138782920
104466899144668992GA22GENIChomozygous138782921
104467207344672074AG15GENIChomozygous138782922
104467294444672945CA23GENICheterozygous154632124
104467578844675853GTGTGTGTGTGCATGTGTGAGGGGTATGTGTGCCTGTGTGTGTGCACGTGTGTGCCTGTGCATAC20GENIChomozygous138681870
104467598344675984AT27GENIChomozygous138782923
104467655544676556A18GENIChomozygous138681871
104467660144676602AT21GENIChomozygous138782924
104467793144677932TC22GENIChomozygous138782925
104467294444672945C23GENICheterozygous144411788