chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78356462683564627CT35GENICheterozygous794466129
78356464383564644TA34GENICheterozygous794466130
78356571683565717AT71GENIChomozygous794466131
78356593483565935AG53GENICpossibly homozygous794466132
78356603683566037TC53GENICpossibly homozygous794466133
78356714483567145TC53GENIChomozygous794466134
78356820283568203CT41GENIChomozygous794466135
78356874483568745AG63GENIChomozygous794466136
78356909183569092GA58GENICpossibly homozygous794466137
78356927283569273AG55GENIChomozygous794466138
78357005383570054TG49GENICpossibly homozygous794466139
78357084983570850CT55GENIChomozygous794466140
78357093983570940CT46GENIChomozygous794466141
78357154283571543TG49GENIChomozygous794466142
78357207483572075CT47GENICpossibly homozygous794466143
78357241383572414GC46GENICpossibly homozygous794466144
78357313583573136CA57GENICpossibly homozygous794466145
78357557383575574TC44GENIChomozygous794466146
78357592183575922GA40GENIChomozygous794466147
78357616983576170TG43GENIChomozygous794466148
78357676283576763AG18GENIChomozygous794466149
78357902083579021TC31GENIChomozygous794466150
78358005483580055AG51GENIChomozygous794466151
78358114783581148GA65GENIChomozygous794466152
78358150483581505GA39GENICpossibly homozygous794466153
78358156183581562TG43GENICpossibly homozygous794466154
78358222983582230GT33GENIChomozygous794466155