chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130297014130297015CG26GENICpossibly homozygous54110940
7130297018130297019TTTCCC13GENIChomozygous54110941
7130297043130297044TC22GENICpossibly homozygous54110942
7130297046130297047TC23GENIChomozygous54110943
7130297237130297238AT28GENIChomozygous54110944
7130297661130297662CCT31GENIChomozygous54110945
7130298181130298182GA40GENIChomozygous54110946
7130298219130298220GA43GENIChomozygous54110947
7130298276130298277AAT45GENIChomozygous54110948