chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41097544910975450GC23GENICheterozygous113250962
41097625610976257TC10GENIChomozygous112497368
41097650210976503GA18GENIChomozygous112497370
41097775210977753CG23GENICpossibly homozygous112497374
41097782310977824TC20GENICheterozygous112497376
41097808010978081GA23GENICpossibly homozygous112497378
41097809410978095AC19GENIChomozygous112497380
41097864210978643GA21GENIChomozygous112497384
41097883610978837AG24GENIChomozygous112497386
41097899410978995CT21GENIChomozygous112497388
41097911910979120GA11GENIChomozygous112497390
41097941710979418GC9GENICpossibly homozygous112497392
41097961110979612CT38GENIChomozygous112497394
41098087110980872AG25GENIChomozygous112497396
41098102210981023TC31GENIChomozygous112497398
41098133310981334CT38GENIChomozygous112497400
41098150410981505CT52GENIChomozygous112497402
41098176310981764CT21GENIChomozygous112497404
41098202010982021TG29GENIChomozygous112497406
41098232910982330CA37GENIChomozygous112497408
41098233910982340TC38GENIChomozygous112497410
41098269410982695AG60GENIChomozygous112497412
41098276210982763CT70GENIChomozygous112497414
41098305110983052CA41GENIChomozygous112497416
41098307210983073CT51GENICheterozygous112497418
41098307410983075CT50GENICheterozygous112497420
41098330410983305GT17GENIChomozygous112497422
41098343510983436CT31GENIChomozygous112497424
41098408410984085TG48GENICpossibly homozygous112497426
41098412510984126TC48GENICpossibly homozygous112497428
41098447710984478CT18GENIChomozygous112497430
41098465910984660TC21GENIChomozygous112497432
41098522610985227TA53GENIChomozygous112497434
41098531010985311CG51GENIChomozygous112497436