chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104615332646153327CT60GENIChomozygous117252569
104615357046153571GC62GENIChomozygous116772312
104615424246154243TC54GENIChomozygous116585154
104615512746155128CA12GENIChomozygous133681297
104615513146155132CG13GENIChomozygous133681298
104615513346155134TG14GENIChomozygous133681299
104615513546155136CG14GENIChomozygous133681300
104615513746155138CG16GENIChomozygous133681301
104615513946155140CG16GENIChomozygous133681302
104615514146155142AG18GENIChomozygous133681303
104615651546156516TC53GENIChomozygous116585162
104615652546156526GA51GENIChomozygous116772314
104615713346157134AC49GENICpossibly homozygous116585164
104615806946158129GGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGAAATCC2GENICheterozygous131901816
104616018846160189TC62GENIChomozygous116585170
104616153846161539TC52GENIChomozygous116585176
104616251546162527GCCAGCAGTCTG55GENIChomozygous133680122
104616317046163171GA60GENIChomozygous117252571
104616319246163193AC61GENICpossibly homozygous116585180
104616578846165789CT69GENIChomozygous116772316
104616764646167647AG61GENIChomozygous116585186
104617145546171456AG62GENIChomozygous116585190
104616779446167803AACAACAAC41GENIChomozygous133680123