chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124026210540262106GC23GENIChomozygous50422525
124026260040262601CCTTTTTTT1GENIChomozygous50543564
124026267640262677CT12GENIChomozygous50422526
124026277940262780AG16GENICheterozygous50543565
124026322440263225AG33GENIChomozygous50422527
124026323040263231CT33GENIChomozygous50422528
124026334840263349AG22GENIChomozygous50202956
124026369240263694TT--8GENICheterozygous50599305
124026369340263694T-8GENICpossibly homozygous50543566
124026436240264363TA39GENIChomozygous50422530
124026444240264443GA24GENIChomozygous50422531
124026480840264809TC38GENIChomozygous50422532
124026541740265418TC14GENIChomozygous50202959