chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124026210540262106GC28GENICpossibly homozygous50422525
124026267640262677CT3GENIChomozygous50422526
124026322440263225AG10GENIChomozygous50422527
124026323040263231CT13GENIChomozygous50422528
124026334840263349AG23GENICpossibly homozygous50202956
124026436240264363TA29GENIChomozygous50422530
124026444240264443GA28GENIChomozygous50422531
124026480840264809TC16GENICpossibly homozygous50422532
124026541740265418TC29GENIChomozygous50202959