chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41032398710323988AC9GENICheterozygous56745839
41032497010324971TC20GENICpossibly homozygous56745842
41032630210326303TC20GENICpossibly homozygous56745843
41032756110327562GA9GENIChomozygous56745848
41032766110327662TTCA16GENIChomozygous56745849
41032771510327716CCA16GENICpossibly homozygous56745850
41032842810328431TGT---4GENICheterozygous56745852
41032842610328427T-4GENICheterozygous58274350
41032842810328429T-4GENICheterozygous58274352
41032866110328662CG14GENIChomozygous56745853
41032920310329204CG15GENIChomozygous56745854