chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46355584063555841GT67GENIChomozygous144667743
46355684963556850AG59GENIChomozygous137066653
46355808963558090AT61GENIChomozygous137066654
46355913963559140AG50GENIChomozygous137066655
46356382763563828AT51GENIChomozygous144667744
46356557863565579CT48GENIChomozygous144667745
46357223663572237CT40GENIChomozygous141625374
46357272463572725GT42GENIChomozygous137066658
46357277063572771GA48GENIChomozygous141625375
46357283163572832CT47GENIChomozygous141625376
46357540063575401AG40GENICheterozygous144350536
46357933363579334TC42GENIChomozygous141625378
46357933663579337CA42GENIChomozygous141625379
46357946663579466TTC13GENICheterozygous141580244
46357946763579467TC13GENICheterozygous145175537
46358010463580105G29GENICheterozygous145175538
46358025963580260T8GENIChomozygous141580245
46358174163581742AT22GENICpossibly homozygous137066659
46358174563581746AT23GENICpossibly homozygous141625380
46358405563584056TC60GENIChomozygous137066661
46358490763584908GT43GENIChomozygous141625381
46358528763585288TC45GENICpossibly homozygous141625382
46358616163586162AG52GENIChomozygous141625383
46358616763586168GA53GENIChomozygous141625384
46358819163588192CT35GENIChomozygous137066662
46358852963588530AT38GENIChomozygous141625385
46358959563589596GA66GENIChomozygous141625386
46359116863591169CG53GENIChomozygous141625387
46356639163566391G60GENIChomozygous144656921
46358415263584153C58GENIChomozygous141580246
46358430863584309T34GENIChomozygous141580247
46358514763585147GAA43GENIChomozygous136887885
46358769963587700T36GENIChomozygous141580248
46357297163572972TG49GENICheterozygous147663339