chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35808680458086805CT15GENIChomozygous112279315
35809107958091080AC28GENIChomozygous112279317
35809467358094674GT28GENIChomozygous111580830
35809479458094795AC25GENIChomozygous111580831
35809485658094857AG18GENIChomozygous112279318
35809645458096455AG31GENIChomozygous111580832
35809657058096571GA35GENIChomozygous112279319
35810562358105624TC44GENIChomozygous111580839
35810576658105767GA31GENIChomozygous112279322
35810578458105785GA31GENIChomozygous112279323
35810708758107088GA42GENIChomozygous112279324
35810807158108072CT33GENIChomozygous112279325
35811802158118022CA19GENIChomozygous111580843
35811804458118045CA17GENIChomozygous111580844
35812495858124959GA23GENIChomozygous112279327
35812784258127843TC11GENIChomozygous112279328
35812958358129584GA18GENIChomozygous112279329
35813124458131245GT31GENIChomozygous112279330
35813632858136329GA30GENIChomozygous112279331
35813643358136434CT26GENICpossibly homozygous119913409
35814132258141323CT22GENIChomozygous112279334
35814533358145334CT23GENIChomozygous112279335
35814564158145642GT32GENIChomozygous112279336
35814649458146495TC31GENIChomozygous111580857
35814937858149379CT13GENIChomozygous111580863
35815039758150398AG28GENIChomozygous111580865
35815055058150551GA28GENIChomozygous112279337
35815100158151002TA22GENIChomozygous112279338
35815404958154050TG33GENIChomozygous112279339
35815516158155162CA28GENIChomozygous112279340
35815527558155276GA37GENIChomozygous112279341
35815676058156761AC23GENIChomozygous111580870
35815739958157400AG23GENIChomozygous111580871
35815931658159317CG38GENIChomozygous111580874