chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5104985774104985775GT8GENIChomozygous55617359
5104989729104989730A-4GENIChomozygous55617362
5104991452104991453AAAATC18GENIChomozygous55617363
5104992805104992806TTA25GENIChomozygous55617364
5104993722104993723AG19GENIChomozygous55617365
5105002730105002731C-20GENICpossibly homozygous55617367
5105004272105004273TTG8GENICheterozygous55617368
5105005288105005289GA30GENIChomozygous55617369
5105005512105005513GC19INTERGENIChomozygous55617370
5105006642105006643CT22INTERGENICheterozygous55617371
5105006644105006645CT21INTERGENICheterozygous55617372
5105006648105006660GTGTGTGTGTGT------------4INTERGENIChomozygous55617373
5105002729105002731CC--20GENICheterozygous55890913