chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35608833356088334AC23GENIChomozygous71894455
35608882556088826TC49GENIChomozygous71894459
35608963856089639CT26GENIChomozygous71894461
35609077956090780TC35GENIChomozygous71894463
35609083956090840CA25GENIChomozygous71894464
35609130856091309AG19GENIChomozygous71894466
35609176756091768CT32GENIChomozygous71894467
35609217456092175GA12GENIChomozygous71894469
35609257556092576GA31GENIChomozygous71894471
35609261456092615AG35GENIChomozygous71894473
35609314256093143CT30GENIChomozygous71894474
35609406456094065TG14GENIChomozygous71894476
35609501856095019AC31GENIChomozygous71894478
35609502456095025GT32GENIChomozygous71894479
35609557956095580CT32GENIChomozygous71894481
35609606956096070TC18GENICpossibly homozygous71894483
35609616956096170CA13GENIChomozygous71894485
35609629456096295GA9GENIChomozygous71894486
35609629656096297GA9GENIChomozygous71894488
35609687156096872GA25GENIChomozygous71894490
35609692756096928GA32GENIChomozygous71894491
35609696256096963CG39GENIChomozygous71894493
35609732456097325AC41GENIChomozygous71894495
35609792756097928TC34GENIChomozygous71894497
35609834956098350CA16GENIChomozygous71894499
35609839756098398AG13GENIChomozygous71894500
35609855456098555AG31GENIChomozygous71894502
35609859956098600TC32GENIChomozygous71894504
35609872756098728AG26GENIChomozygous71894505
35609879456098795GC29GENIChomozygous71894507
35609883056098831CT26GENIChomozygous71894509
35609902156099022TG21GENIChomozygous71894511
35609905556099056CT20GENIChomozygous71894512
35609938156099382GA32GENIChomozygous71894514
35609944356099444TC32GENIChomozygous71894516
35609995656099957CT32GENICpossibly homozygous71894518
35610017356100174CA43GENIChomozygous71894520
35610021756100218CT37GENIChomozygous71894521
35610070156100702AT26GENIChomozygous71894523
35610119756101198TC25GENIChomozygous71894525
35610240656102407AG18GENIChomozygous71894527
35610246156102462TC28GENIChomozygous71894528
35610247556102476CT30GENIChomozygous71894530