chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118680557118680558AG26GENICheterozygous54079778
7118680619118680620CT30GENICheterozygous54079779
7118687138118687139TC33GENICheterozygous54079830
7118687192118687193CT41GENICheterozygous54079831
7118689943118689944CT27GENICheterozygous54079868
7118689995118689996CT40GENICheterozygous54079869
7118690008118690009AC41GENICheterozygous54079870
7118690035118690036CT37GENICheterozygous54079871
7118690408118690409AC19GENICheterozygous54079876
7118690708118690709TC34GENICheterozygous54079877
7118690747118690748CT32GENICheterozygous56484007
7118690903118690904AG57GENICheterozygous54079878
7118691071118691072AG42GENICheterozygous54079879
7118691161118691162CG34GENICheterozygous54079882
7118691257118691258GC28GENICheterozygous56484008
7118691293118691294GA22GENICheterozygous54079884
7118691431118691432TC44GENICheterozygous54079885