chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52414412524144126CA23GENIChomozygous56280494
52414444124144442GA16GENIChomozygous56280495
52414485124144852AG20GENIChomozygous56280496
52414593724145938CT25GENIChomozygous56280497
52414598324145984AG18GENIChomozygous56280498
52414604824146049GC31GENIChomozygous56280499
52414605424146055AG32GENIChomozygous56280500
52414613524146136GC19GENIChomozygous56280501
52414693224146935ACT---19GENIChomozygous56280502
52414694224146943CT20GENIChomozygous56280503
52414720824147209CT15GENIChomozygous56280504
52414722624147227AC15GENIChomozygous56280505
52414727124147272TG20GENIChomozygous56280506
52414736724147368GA27GENIChomozygous56280507
52414751024147511AG31GENIChomozygous56280508
52414755224147553CT28GENIChomozygous56280509
52414757324147574TC27GENIChomozygous56280510
52414772424147725CG37GENIChomozygous56206185
52414793024147931TA19GENIChomozygous56280511
52414799924148008ATATTATGG---------17GENIChomozygous56280512
52414800924148010AC13GENIChomozygous56402643
52414805424148055GA20GENIChomozygous56280513
52414811124148112TC14GENIChomozygous56206186
52414814024148141A-14GENIChomozygous56280514
52414846224148463AG10GENIChomozygous56280515
52414952024149521GA25GENIChomozygous56280516
52414956924149570TC18GENIChomozygous56206188
52414959724149598AG14GENIChomozygous56206189
52414985324149854GA33GENIChomozygous56280517
52415015324150154GA35GENIChomozygous56280518
52415168924151690TTA18GENIChomozygous56280519
52415202324152024T-22GENICpossibly homozygous56206193
52415281824152819TC21GENIChomozygous56206194
52415314824153149TC31GENIChomozygous56206196