chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5104985774104985775GT19GENIChomozygous55617359
5104987709104987710GGT11GENICheterozygous55617361
5104989729104989730A-23GENIChomozygous55617362
5104991452104991453AAAATC17GENICpossibly homozygous55617363
5104992805104992806TTA27GENIChomozygous55617364
5104993722104993723AG17GENIChomozygous55617365
5104994867104994868TG17GENICheterozygous55617366
5105002730105002731C-8GENICheterozygous55617367
5105004272105004273TTG2GENICheterozygous55617368
5105005288105005289GA22GENIChomozygous55617369
5105005512105005513GC22INTERGENIChomozygous55617370
5105006642105006643CT18INTERGENICheterozygous55617371
5105006644105006645CT17INTERGENICheterozygous55617372
5105006648105006660GTGTGTGTGTGT------------5INTERGENIChomozygous55617373
5105002729105002731CC--8GENICheterozygous55890913