chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118772235487722355G10GENIChomozygous128931816
118772472787724728TC61GENIChomozygous115929277
118772332787723328TC41GENIChomozygous115929271
118772451387724514CA43GENIChomozygous115929273
118772472687724727TG62GENIChomozygous115929275
118772556887725569CG14GENIChomozygous123545467
118772656387726564AC35GENIChomozygous115929279
118772660287726603AG46GENIChomozygous115929281
118772697187726972AG43GENIChomozygous115929283
118772986787729868GA42GENIChomozygous115929285
118772996487729965G26GENIChomozygous128931817
118772996687729967GT26GENIChomozygous115929287
118773006187730062G36GENIChomozygous128931818
118773010987730110CT28GENIChomozygous115929289
118773011987730120CA30GENIChomozygous115929291
118773041987730420CT41GENICpossibly homozygous123545476
118773042087730421TG41GENICpossibly homozygous123545477
118773086487730864T8GENIChomozygous128931819
118773086887730868AGAAC9GENICheterozygous128931821
118773129887731299TG32GENIChomozygous115929295
118773196987731970AG48GENIChomozygous115929297
118773220687732207AG48GENIChomozygous115929299
118773341487733415TC42GENIChomozygous115929301
118773089387730894GA15GENIChomozygous116362490
118772556687725567CG15GENICheterozygous128946490
118773040387730404TA42GENIChomozygous118171562
118773042587730426GC40GENICpossibly homozygous118171563