chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35608833356088334AC28GENIChomozygous71894455
35608882556088826TC21GENIChomozygous71894459
35608963856089639CT34GENIChomozygous71894461
35609077956090780TC24GENIChomozygous71894463
35609083956090840CA17GENIChomozygous71894464
35609130856091309AG8GENIChomozygous71894466
35609176756091768CT25GENIChomozygous71894467
35609217456092175GA17GENIChomozygous71894469
35609257556092576GA12GENIChomozygous71894471
35609261456092615AG15GENIChomozygous71894473
35609314256093143CT23GENIChomozygous71894474
35609406456094065TG17GENIChomozygous71894476
35609501856095019AC6GENICheterozygous71894478
35609502456095025GT7GENICpossibly homozygous71894479
35609557956095580CT43GENIChomozygous71894481
35609606956096070TC30GENIChomozygous71894483
35609616956096170CA37GENIChomozygous71894485
35609629456096295GA42GENIChomozygous71894486
35609629656096297GA42GENIChomozygous71894488
35609687156096872GA18GENIChomozygous71894490
35609692756096928GA23GENIChomozygous71894491
35609696256096963CG21GENIChomozygous71894493
35609732456097325AC30GENIChomozygous71894495
35609792756097928TC20GENIChomozygous71894497
35609834956098350CA30GENIChomozygous71894499
35609839756098398AG33GENIChomozygous71894500
35609855456098555AG22GENIChomozygous71894502
35609859956098600TC23GENIChomozygous71894504
35609872756098728AG35GENIChomozygous71894505
35609879456098795GC25GENIChomozygous71894507
35609883056098831CT29GENIChomozygous71894509
35609902156099022TG21GENIChomozygous71894511
35609905556099056CT11GENIChomozygous71894512
35609938156099382GA31GENIChomozygous71894514
35609944356099444TC35GENIChomozygous71894516
35609995656099957CT24GENIChomozygous71894518
35610017356100174CA22GENIChomozygous71894520
35610021756100218CT37GENIChomozygous71894521
35610070156100702AT26GENIChomozygous71894523
35610119756101198TC20GENIChomozygous71894525
35610240656102407AG6GENIChomozygous71894527
35610246156102462TC7GENIChomozygous71894528
35610247556102476CT11GENIChomozygous71894530