chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71265622812656229TC13GENIChomozygous115570310
71265743512657436AG5GENIChomozygous118251052
71265936712659368CA10GENIChomozygous115570314
71265970312659704TC15GENIChomozygous115570315
71266127012661271AG9GENIChomozygous115570319
71266216912662170AT9GENIChomozygous115570320
71266234912662350TC8GENIChomozygous116274828
71266240212662403CT7GENIChomozygous115570321
71266244512662446TC6GENIChomozygous115570322
71266251012662511CG7GENIChomozygous115570324
71266326612663267GC8GENICpossibly homozygous116274832