chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102901436129014362GA20GENIChomozygous116538948
102901513429015135TC29GENIChomozygous116538950
102901529229015292GC25GENIChomozygous128801468
102901731629017317AG20GENIChomozygous116538952
102901914929019150AG26GENIChomozygous116538954
102902030829020309CT9GENIChomozygous116538956
102902032829020329GT8GENICpossibly homozygous116538958
102902162629021626T25GENIChomozygous128801469
102902192029021921GA12GENIChomozygous116538960
102902228429022285CA25GENIChomozygous116538962
102902228929022290GA27GENIChomozygous116538964
102902231429022315AC25GENIChomozygous116538966
102902244429022452CGCGCACG19GENIChomozygous128801470
102902245229022453CT19GENIChomozygous116538968
102902246429022528CACACGCACGCGCACACGCACGCGCACACACACGCGCACACACACACACACACACACACACACA22GENIChomozygous128801471
102902379329023794AG20GENIChomozygous116538970
102902388329023884CA17GENIChomozygous116538972
102902392029023921CT16GENIChomozygous116538974
102902398329023984CT21GENIChomozygous116538976
102902398529023986GA22GENIChomozygous116538978
102902398729023988CT22GENIChomozygous116538980
102902403429024035GT22GENIChomozygous116538982
102902404029024041GC20GENIChomozygous116538984
102902409729024098GA13GENIChomozygous116538986
102902410829024109C10GENIChomozygous128801472
102902411129024111AG10GENIChomozygous128801473
102902419229024193CT5GENIChomozygous116538988
102902427529024276T14GENIChomozygous128801474
102902433329024334T18GENIChomozygous128801475
102902457229024572A6GENIChomozygous128801476
102902488429024885GA21GENIChomozygous116538990
102902515529025156CG20GENIChomozygous116538992
102902517429025174G17GENIChomozygous128801478
102902553329025534AG17GENIChomozygous116538994
102902589129025892CG14GENIChomozygous116538996