chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116500772116500773TC42GENIChomozygous54075725
7116501324116501325CCA18GENIChomozygous54075726
7116501470116501471CT18GENIChomozygous54075727
7116501473116501474CT17GENIChomozygous54075728
7116501489116501490CG13GENIChomozygous54075729
7116501502116501503CA9GENICpossibly homozygous54075730
7116501511116501512CG10GENIChomozygous54231312
7116501520116501521CG9GENIChomozygous54231313
7116501523116501524CG10GENICheterozygous54231314
7116501535116501536CG9GENIChomozygous54231315
7116501543116501544CG11GENIChomozygous54075731
7116501548116501549CG11GENIChomozygous54075732
7116501555116501556CG9GENIChomozygous54075733