chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104615329146153292TC70GENIChomozygous116585152
104615424246154243TC47GENIChomozygous116585154
104615429346154294GT48GENIChomozygous116585156
104615485846154861ATT22GENIChomozygous128814154
104615498846154988T20GENIChomozygous128814155
104615508046155084ACTC11GENICheterozygous128814156
104615518346155184GT23GENIChomozygous117312531
104615651546156516TC47GENIChomozygous116585162
104615713346157134AC49GENIChomozygous116585164
104615782346157824GT51GENIChomozygous116585166
104615797446157975TG56GENIChomozygous116585168
104615822346158224AC27GENICheterozygous117993462
104615824346158244AC29GENICheterozygous118036384
104615828346158284AC8GENICpossibly homozygous118122949
104616018846160189TC50GENICpossibly homozygous116585170
104616108646161087GA49GENIChomozygous116585172
104616113446161135AG60GENIChomozygous116585174
104616153846161539TC45GENIChomozygous116585176
104616310446163105CT56GENIChomozygous116585178
104616319246163193AC53GENIChomozygous116585180
104616591146165912GA54GENIChomozygous116585182
104616601346166014GA53GENIChomozygous116585184
104616764646167647AG67GENIChomozygous116585186
104616848846168489GA55GENIChomozygous116585188
104617134346171343CCAC46GENIChomozygous128814158
104617145546171456AG46GENIChomozygous116585190
104615806946158129GGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGAAATCC10GENICpossibly homozygous131901816
104615830646158307T5GENIChomozygous131901817
104615830946158310TC5GENIChomozygous131905500