chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124026210540262106GC27GENIChomozygous50422525
124026260040262601CCTTTTTTT3GENIChomozygous50543564
124026267640262677CT10GENIChomozygous50422526
124026277940262780AG8GENIChomozygous50543565
124026322440263225AG28GENIChomozygous50422527
124026323040263231CT33GENIChomozygous50422528
124026334840263349AG29GENIChomozygous50202956
124026369340263694T-3GENIChomozygous50543566
124026436240264363TA21GENIChomozygous50422530
124026444240264443GA19GENIChomozygous50422531
124026480840264809TC28GENIChomozygous50422532
124026541740265418TC22GENIChomozygous50202959