chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105724070257240703AAT32GENICpossibly homozygous51658247
105724203257242033AG29GENIChomozygous51461124
105724562057245621GC33GENIChomozygous51461133
105724650457246505TG20GENIChomozygous51658249
105724671157246712TA33GENIChomozygous51461135