chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12628876628877GT66GENIChomozygous781722434
12629151629152CT65GENIChomozygous781722435
12631942631943CA55GENICpossibly homozygous781722436
12632987632988TC53GENICpossibly homozygous781722437
12632993632994TA53GENICpossibly homozygous781722438
12634650634651AG44GENIChomozygous781722439
12637190637191CA29GENIChomozygous781722440
12639307639308CT76GENICpossibly homozygous781722441
12640764640765AG68GENICheterozygous781722442
12641063641064AT62GENICpossibly homozygous781722443
12648151648152CA25GENIChomozygous781722444