chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52414412524144126CA20GENIChomozygous56280494
52414444124144442GA19GENIChomozygous56280495
52414485124144852AG18GENIChomozygous56280496
52414593724145938CT21GENIChomozygous56280497
52414598324145984AG17GENIChomozygous56280498
52414604824146049GC19GENIChomozygous56280499
52414605424146055AG18GENIChomozygous56280500
52414613524146136GC21GENIChomozygous56280501
52414693224146935ACT---12GENIChomozygous56280502
52414694224146943CT13GENIChomozygous56280503
52414720824147209CT24GENIChomozygous56280504
52414722624147227AC24GENIChomozygous56280505
52414727124147272TG27GENIChomozygous56280506
52414736724147368GA18GENIChomozygous56280507
52414751024147511AG22GENIChomozygous56280508
52414755224147553CT20GENIChomozygous56280509
52414757324147574TC17GENIChomozygous56280510
52414772424147725CG12GENIChomozygous56206185
52414793024147931TA16GENICpossibly homozygous56280511
52414799924148008ATATTATGG---------7GENIChomozygous56280512
52414805424148055GA12GENIChomozygous56280513
52414811124148112TC16GENIChomozygous56206186
52414814024148141A-14GENIChomozygous56280514
52414846224148463AG14GENIChomozygous56280515
52414952024149521GA27GENIChomozygous56280516
52414956924149570TC34GENIChomozygous56206188
52414959724149598AG32GENIChomozygous56206189
52414985324149854GA34GENIChomozygous56280517
52415015324150154GA15GENIChomozygous56280518
52415168924151690TTA12GENIChomozygous56280519
52415202324152024T-20GENIChomozygous56206193
52415281824152819TC20GENIChomozygous56206194
52415314824153149TC11GENIChomozygous56206196