chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109906747109906748TC38GENIChomozygous116719308
10109906992109906993TA35GENICpossibly homozygous116719310
10109906993109906994CA35GENIChomozygous116719312
10109908046109908047CT49GENIChomozygous116719314