chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1192300248192300249GA89GENICpossibly homozygous61025804
1192300560192300561GA73GENICpossibly homozygous61025805
1192300595192300596GA51GENICpossibly homozygous61025806
1192300638192300639GGGTGTGTGTGT9GENIChomozygous61025807
1192300888192300890CG--49GENIChomozygous61025809
1192300889192300893GCTG----49GENIChomozygous61025810
1192300938192300939TC60GENIChomozygous61025811
1192301009192301010CT54GENIChomozygous61025812
1192301498192301499TC57GENIChomozygous61025813
1192301713192301714AACTC55GENIChomozygous61025814
1192301903192301904GA59GENIChomozygous61025815
1192301965192301966AAT62GENIChomozygous61025816