chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264059544264059545CA41GENICpossibly homozygous108782979
1264060180264060181TA25GENIChomozygous108782980
1264061466264061467TC31GENIChomozygous108635000
1264061991264061992GA11GENIChomozygous108635002
1264062067264062068CA5GENIChomozygous109377213
1264062070264062071CA4GENIChomozygous120813381
1264062297264062298TC22GENIChomozygous108635006
1264062381264062382CT27GENIChomozygous108635007
1264062501264062502AG20GENIChomozygous108635009
1264062858264062859GT33GENIChomozygous108635011
1264064003264064004AG23GENIChomozygous108635013
1264064234264064235TG33GENIChomozygous108635015
1264064623264064624GA31GENIChomozygous108782981
1264064641264064642CT34GENIChomozygous108635017
1264064988264064989AG38GENIChomozygous108635019
1264066698264066699TC33GENIChomozygous108635024
1264067060264067061TC23GENIChomozygous108635026
1264067293264067294AG17GENIChomozygous108635028
1264068461264068462TG22GENIChomozygous108782983
1264068572264068573GA32GENIChomozygous108635032
1264069891264069892GA36GENIChomozygous108782984
1264070790264070791CT28GENICpossibly homozygous108782985
1264071209264071210CT29GENIChomozygous108782986
1264071386264071387GA34GENIChomozygous108635036