chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108165767681657677TA29GENIChomozygous116811936
108165770181657702AG30GENIChomozygous116811938
108165773681657737GA24GENIChomozygous116811940
108165873381658734GA24GENIChomozygous116811942
108165927681659277GA17GENIChomozygous116811944
108165928081659281TC16GENIChomozygous116657318
108165938481659385TC18GENIChomozygous116811946
108165950781659508GA19GENIChomozygous116811948
108165960381659604GT24GENIChomozygous116811950
108165960981659610AT25GENIChomozygous116811952
108166039781660398CT35GENIChomozygous116811954
108166096381660964AT31GENIChomozygous116811956
108166106081661061GA19GENIChomozygous116811958
108166111781661118AC19GENIChomozygous116811960
108166138981661390AG18GENIChomozygous116811962
108166177481661775GT32GENIChomozygous116811964
108166181281661813AG21GENIChomozygous116811966
108166184281661843GA19GENIChomozygous116811968
108166219081662191CT25GENIChomozygous116811970
108166260181662602GA26GENIChomozygous116811972
108166264181662642GA27GENIChomozygous116811974
108166324481663245AG23GENIChomozygous116811976
108166350781663508TC20GENIChomozygous116811978
108166384781663848TC16GENIChomozygous116811980
108166411381664114TC26GENIChomozygous116657326
108166454881664549GA26GENIChomozygous116811982
108166569981665700AG15GENIChomozygous116657328
108166589581665896GA17GENIChomozygous116811984
108166646981666470TC32GENIChomozygous116657330
108166012981660130AG27GENIChomozygous116897938
108166115781661158GA24GENICheterozygous118068872