chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6145373027145373028CA54GENIChomozygous54764273
6145373955145373956AG60GENIChomozygous54764274
6145374721145374722TC72GENIChomozygous54764275
6145374727145374728TC70GENIChomozygous54764276
6145374770145374771TC53GENIChomozygous54764277
6145375121145375122AT46GENIChomozygous54764278
6145375122145375123TC48GENICpossibly homozygous54764279
6145375485145375486GA31GENIChomozygous54764280
6145375779145375780TC56GENIChomozygous54764281
6145375865145375866CT50GENIChomozygous54764282
6145375868145375869TC46GENIChomozygous54764283
6145375904145375905TG46GENICheterozygous54764284
6145376153145376154TG62GENIChomozygous54764285
6145376732145376733GT33GENIChomozygous54764286
6145377031145377035GTTT----36GENIChomozygous54764287
6145377370145377371GA57GENIChomozygous54764288
6145377704145377705TC54GENIChomozygous54764289
6145377931145377932AG61GENIChomozygous54764290
6145378055145378056TC34GENIChomozygous54764291
6145378077145378078TC36GENIChomozygous54764292
6145378082145378083GA30GENIChomozygous54764293
6145378499145378500TC32GENIChomozygous54764294
6145378526145378527G-1GENIChomozygous54764295
6145378568145378569GA33GENIChomozygous54764296
6145379108145379109GA57GENIChomozygous54764297
6145379142145379143AG49GENIChomozygous54764298
6145379188145379189GT44GENICpossibly homozygous54764299
6145379201145379205GTGT----41GENIChomozygous54764300
6145379794145379795CT48GENIChomozygous54764301
6145380032145380033TC70GENICpossibly homozygous54764302
6145380277145380278CT42GENIChomozygous54764303
6145380578145380579AAAGG30GENIChomozygous54764304
6145380632145380633GA45GENIChomozygous54764305
6145380904145380905GA42GENIChomozygous54764306
6145380910145380911CT42GENICpossibly homozygous54764307
6145380976145380977AG44GENIChomozygous54764308
6145381069145381070CT53GENIChomozygous54764309
6145385015145385017CA--10GENICheterozygous54764310
6145388575145388576CT30GENIChomozygous54764311