chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104615329146153292TC18GENIChomozygous116585152
104615424246154243TC20GENIChomozygous116585154
104615429346154294GT26GENIChomozygous116585156
104615651546156516TC32GENIChomozygous116585162
104615713346157134AC25GENIChomozygous116585164
104615782346157824GT25GENIChomozygous116585166
104615797446157975TG32GENIChomozygous116585168
104615485846154861ATT22GENIChomozygous128814154
104615498846154988T16GENIChomozygous128814155
104615518346155184GT16GENIChomozygous117312531
104615806946158129GGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGAAATCC8GENICheterozygous131901816
104615828346158284AC6GENICheterozygous118122949
104616018846160189TC16GENIChomozygous116585170
104616108646161087GA31GENIChomozygous116585172
104616113446161135AG33GENIChomozygous116585174
104616153846161539TC33GENIChomozygous116585176
104616310446163105CT26GENIChomozygous116585178
104616319246163193AC35GENIChomozygous116585180
104616591146165912GA24GENIChomozygous116585182
104616601346166014GA26GENIChomozygous116585184
104617134346171343CCAC23GENIChomozygous128814158
104616764646167647AG31GENIChomozygous116585186
104616848846168489GA32GENIChomozygous116585188
104617145546171456AG20GENIChomozygous116585190