chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189107153189107153TCTGTGTGTC35GENICpossibly homozygous134800143
2189110991189110992GC61GENIChomozygous134806278
2189111268189111277AGGGTCCTG56GENIChomozygous132017793
2189111083189111084TG56GENIChomozygous110170825
2189109580189109581AG53GENIChomozygous110170824
2189113079189113080CT64GENIChomozygous110170829
2189112973189112974GA62GENIChomozygous110170827
2189113225189113226AG51GENIChomozygous110170831
2189113249189113250TC56GENIChomozygous110170833
2189113439189113440CT54GENIChomozygous110170835
2189114249189114250CT36GENIChomozygous134806279
2189115032189115033CT39GENIChomozygous110804867
2189114996189114996T40GENIChomozygous131298145
2189107458189107459G34GENIChomozygous127717637
2189112725189112731CTGCCT57GENIChomozygous127717638