chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41032398710323988AC28GENICpossibly homozygous56745839
41032406610324067AG29GENICheterozygous56745840
41032445410324460AACAAC------8GENIChomozygous56745841
41032497010324971TC78GENIChomozygous56745842
41032630210326303TC46GENIChomozygous56745843
41032741110327433TGTGTGTGTGTGTGTGTGTGTG----------------------2GENIChomozygous56745844
41032745410327455TG20GENIChomozygous56745845
41032745610327457AG19GENIChomozygous56745846
41032746410327465AG28GENICpossibly homozygous56745847
41032756110327562GA50GENIChomozygous56745848
41032766110327662TTCA38GENIChomozygous56745849
41032771510327716CCA46GENIChomozygous56745850
41032842610328429TGT---6GENICheterozygous56745851
41032842810328431TGT---4GENIChomozygous56745852
41032866110328662CG46GENIChomozygous56745853
41032920310329204CG69GENIChomozygous56745854