chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105723917257239173TTCTTC2GENIChomozygous52503018
105724070257240703AAT23GENICpossibly homozygous51658247
105724203257242033AG21GENIChomozygous51461124
105724562057245621GC29GENIChomozygous51461133
105724650457246505TG31GENIChomozygous51658249
105724671157246712TA26GENIChomozygous51461135