chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52414412524144126CA7GENIChomozygous56280494
52414444124144442GA6GENIChomozygous56280495
52414485124144852AG9GENIChomozygous56280496
52414593724145938CT12GENIChomozygous56280497
52414598324145984AG10GENIChomozygous56280498
52414604824146049GC10GENIChomozygous56280499
52414605424146055AG8GENIChomozygous56280500
52414613524146136GC13GENIChomozygous56280501
52414693224146935ACT---9GENIChomozygous56280502
52414694224146943CT9GENIChomozygous56280503
52414720824147209CT8GENIChomozygous56280504
52414722624147227AC7GENIChomozygous56280505
52414727124147272TG13GENIChomozygous56280506
52414736724147368GA12GENIChomozygous56280507
52414751024147511AG11GENIChomozygous56280508
52414755224147553CT10GENIChomozygous56280509
52414757324147574TC10GENIChomozygous56280510
52414772424147725CG14GENIChomozygous56206185
52414793024147931TA15GENIChomozygous56280511
52414799924148008ATATTATGG---------10GENIChomozygous56280512
52414800924148010AC7GENIChomozygous56402643
52414805424148055GA7GENIChomozygous56280513
52414811124148112TC9GENIChomozygous56206186
52414814024148141A-7GENIChomozygous56280514
52414846224148463AG6GENIChomozygous56280515
52414952024149521GA17GENIChomozygous56280516
52414956924149570TC16GENIChomozygous56206188
52414959724149598AG16GENIChomozygous56206189
52414985324149854GA13GENIChomozygous56280517
52415015324150154GA7GENIChomozygous56280518
52415168924151690TTA6GENIChomozygous56280519
52415202324152024T-7GENIChomozygous56206193
52415281824152819TC9GENIChomozygous56206194
52415314824153149TC9GENICpossibly homozygous56206196