chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123465397123465398GA11GENIChomozygous116082286
7123465532123465533CG6GENIChomozygous116082287
7123467447123467448AG6GENIChomozygous116082289
7123467538123467539TC8GENIChomozygous116082290
7123467686123467687GC12GENIChomozygous116082291
7123467698123467699TC13GENIChomozygous116082292
7123468790123468791TA10GENIChomozygous116082294
7123470336123470337AG7GENIChomozygous116082295
7123471495123471496CT10GENIChomozygous116082296
7123472140123472141CA17GENIChomozygous115863190
7123473032123473033TC20GENIChomozygous115863196
7123473830123473831AT7GENIChomozygous115863206
7123474407123474408GA17GENIChomozygous118286437
7123474408123474409AG17GENIChomozygous118286439
7123474691123474692TC27GENIChomozygous116082297
7123474907123474908TC20GENIChomozygous115863208
7123474969123474970CA18GENICpossibly homozygous116082298
7123475463123475464CA5GENIChomozygous116082299