chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41032398710323988AC26GENIChomozygous56745839
41032406610324067AG36GENICheterozygous56745840
41032445410324460AACAAC------14GENIChomozygous56745841
41032497010324971TC35GENIChomozygous56745842
41032630210326303TC25GENIChomozygous56745843
41032741110327433TGTGTGTGTGTGTGTGTGTGTG----------------------10GENICheterozygous56745844
41032745410327455TG19GENIChomozygous56745845
41032745610327457AG20GENIChomozygous56745846
41032746410327465AG27GENIChomozygous56745847
41032756110327562GA41GENIChomozygous56745848
41032766110327662TTCA32GENIChomozygous56745849
41032771510327716CCA28GENIChomozygous56745850
41032842610328429TGT---11GENICheterozygous56745851
41032842810328431TGT---17GENICpossibly homozygous56745852
41032866110328662CG25GENIChomozygous56745853
41032920310329204CG36GENIChomozygous56745854