chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35608833356088334AC34GENIChomozygous71894455
35608882556088826TC46GENIChomozygous71894459
35608963856089639CT26GENIChomozygous71894461
35609077956090780TC58GENIChomozygous71894463
35609083956090840CA46GENIChomozygous71894464
35609130856091309AG33GENIChomozygous71894466
35609176756091768CT40GENIChomozygous71894467
35609217456092175GA18GENIChomozygous71894469
35609257556092576GA34GENIChomozygous71894471
35609261456092615AG26GENIChomozygous71894473
35609314256093143CT43GENIChomozygous71894474
35609406456094065TG14GENIChomozygous71894476
35609501856095019AC37GENIChomozygous71894478
35609502456095025GT39GENIChomozygous71894479
35609557956095580CT35GENIChomozygous71894481
35609606956096070TC26GENICpossibly homozygous71894483
35609616956096170CA30GENIChomozygous71894485
35609629456096295GA28GENICpossibly homozygous71894486
35609629656096297GA29GENICpossibly homozygous71894488
35609687156096872GA59GENIChomozygous71894490
35609692756096928GA50GENIChomozygous71894491
35609696256096963CG55GENIChomozygous71894493
35609732456097325AC61GENIChomozygous71894495
35609792756097928TC33GENIChomozygous71894497
35609834956098350CA19GENIChomozygous71894499
35609839756098398AG21GENIChomozygous71894500
35609855456098555AG46GENIChomozygous71894502
35609859956098600TC38GENIChomozygous71894504
35609872756098728AG42GENIChomozygous71894505
35609879456098795GC44GENIChomozygous71894507
35609883056098831CT44GENIChomozygous71894509
35609902156099022TG42GENIChomozygous71894511
35609905556099056CT29GENIChomozygous71894512
35609938156099382GA52GENIChomozygous71894514
35609944356099444TC55GENIChomozygous71894516
35609995656099957CT60GENIChomozygous71894518
35610017356100174CA62GENIChomozygous71894520
35610021756100218CT55GENIChomozygous71894521
35610070156100702AT33GENIChomozygous71894523
35610119756101198TC32GENIChomozygous71894525
35610240656102407AG33GENIChomozygous71894527
35610246156102462TC32GENIChomozygous71894528
35610247556102476CT33GENIChomozygous71894530