chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206702330206702331TG15GENICpossibly homozygous61067591
1206703129206703130GA26GENICheterozygous61067592
1206703526206703527CCAAAT5GENIChomozygous61067593
1206704922206704923CT27GENICpossibly homozygous61067594
1206705237206705238AG18GENIChomozygous61067595
1206705702206705703AT20GENIChomozygous61067596
1206708195206708196CT23GENICpossibly homozygous61067597