chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112418172624181727GA14GENIChomozygous953129583
112418279024182791GA20GENIChomozygous953129584
112418400424184005GT27GENIChomozygous953129585
112418400724184008TG26GENIChomozygous953129586
112418445924184460CA25GENIChomozygous953129587
112418490724184908AG11GENIChomozygous953129588
112418531824185319CA25GENIChomozygous953129589
112418567024185671TC28GENIChomozygous953129590
112418668324186684AT29GENIChomozygous953129591
112418684124186842GA30GENIChomozygous953129592
112418693024186931CT30GENIChomozygous953129593
112418718524187186AC20GENIChomozygous953129594
112418761624187617CT31GENIChomozygous953129595
112418796924187970CT31GENIChomozygous953129596
112418816124188162GA22GENIChomozygous953129597
112418862824188629AC27GENIChomozygous953129598
112418968824189689TC19GENIChomozygous953129599
112419055224190553CT27GENIChomozygous953129600
112419055524190556GA30GENIChomozygous953129601
112419071024190711AT37GENIChomozygous953129602
112419206224192063CG24GENIChomozygous953129603
112419282224192823CT22GENIChomozygous953129604