chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
727537682753769CG40GENIChomozygous118399333
727543782754379CT49GENICpossibly homozygous116311436
727545372754538GA47GENIChomozygous118399334
727548992754900GA53GENIChomozygous118399335
727554472755448GA26GENIChomozygous118399336
727563472756348GC26GENIChomozygous118399337
727564492756450TC30GENIChomozygous118399338
727589042758905AT31GENIChomozygous116311439
727589722758973GC31GENIChomozygous115545780
727595832759584TG14GENIChomozygous118399339
727628332762834AG24GENIChomozygous115545785
727691072769108GA42GENIChomozygous118399340
727699062769907CT22GENIChomozygous118399341
727730672773068CT21GENICpossibly homozygous118399342
727730712773072CT19GENICheterozygous118399343
727732902773291AG46GENIChomozygous116311483
727739492773950TA22GENIChomozygous118399344
727747142774715CT20GENIChomozygous115545860
727750802775081GA15GENIChomozygous118399345
727758972775898GA37GENIChomozygous118399346
727759582775959CT40GENIChomozygous118399347
727781742778175TC36GENICpossibly homozygous115545862
727783912778392TC32GENICpossibly homozygous115545864
727784332778434TA34GENICpossibly homozygous115545866
727785222778523TC36GENICpossibly homozygous115545869
727787232778724AG31GENICpossibly homozygous115545871