chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104676917246769173TC19GENIChomozygous116586604
104676931346769314AC23GENIChomozygous116586606
104677020346770204AG35GENIChomozygous116586608
104677092146770922GC30GENIChomozygous116586610
104677171846771719AG28GENIChomozygous116586612
104677217146772172CT23GENIChomozygous116586614
104677309446773095GA25GENIChomozygous116586616
104677326846773269CT27GENIChomozygous116586618
104677346046773461GC20GENIChomozygous116586620
104677649446776495AT28GENIChomozygous116586622
104677744946777450CT25GENIChomozygous116586624
104677824346778244GA28GENIChomozygous116586626
104677913046779131CT18GENIChomozygous116586628
104678004146780042TG28GENIChomozygous116586630
104678208146782082AC34GENIChomozygous116586632
104678263746782638GA23GENIChomozygous116586634
104678328946783290GA23GENIChomozygous116586636
104678354046783541GA12GENIChomozygous116586638