chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130297014130297015CG20GENICpossibly homozygous54110940
7130297018130297019TTTCCC14GENIChomozygous54110941
7130297043130297044TC18GENICpossibly homozygous54110942
7130297046130297047TC17GENIChomozygous54110943
7130297237130297238AT57GENIChomozygous54110944
7130297661130297662CCT52GENIChomozygous54110945
7130298181130298182GA54GENIChomozygous54110946
7130298219130298220GA48GENIChomozygous54110947
7130298276130298277AAT56GENIChomozygous54110948