chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174476032844760329TG102GENICpossibly homozygous111307098
174476065644760657CT98GENIChomozygous111054196
174476068344760684GA102GENIChomozygous111054198
174476224244762243TC71GENIChomozygous111054200