chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203667248203667249CT20GENIChomozygous110210692
2203667280203667281CG18GENIChomozygous110210695
2203667288203667289AC17GENIChomozygous110210696
2203667302203667303AT20GENIChomozygous110210697
2203667309203667310CT17GENIChomozygous110210698
2203669934203669935AG38GENIChomozygous111004728
2203671934203671935AG18GENIChomozygous110210705
2203672620203672621GT26GENIChomozygous111004731
2203674025203674026AG22GENIChomozygous110210711
2203678047203678048GA20GENICpossibly homozygous111004733