chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78160735781607358TC54GENIChomozygous808038774
78160736381607364GT52GENICpossibly homozygous808038775
78160740681607407TC51GENIChomozygous808038776
78160741481607415TC53GENIChomozygous808038777
78160779481607795TG55GENIChomozygous808038778
78160803481608035TA26GENIChomozygous808038779
78160871681608717CG50GENIChomozygous808038780
78160879281608793TC48GENIChomozygous808038781
78160889981608900TC64GENICheterozygous808038782
78160926581609266CT39GENIChomozygous808038783
78160990781609908TG47GENIChomozygous808038784
78161014981610150TC50GENIChomozygous808038785
78161021481610215GA58GENIChomozygous808038786
78161033681610337GA49GENIChomozygous808038787
78161040981610410TA40GENICpossibly homozygous808038788
78161077981610780AG54GENICpossibly homozygous808038789
78161110781611108CA47GENIChomozygous808038790
78161138081611381GA49GENIChomozygous808038791
78161144681611447CG45GENICheterozygous808038792
78161216681612167AG50GENIChomozygous808038793
78161219481612195TA52GENIChomozygous808038794
78161254881612549AG37GENIChomozygous808038795
78161269081612691AG59GENIChomozygous808038796