chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124026210540262106GC26GENICpossibly homozygous50422525
124026267640262677CT4GENIChomozygous50422526
124026322440263225AG13GENIChomozygous50422527
124026323040263231CT18GENIChomozygous50422528
124026334840263349AG20GENIChomozygous50202956
124026436240264363TA20GENIChomozygous50422530
124026444240264443GA22GENIChomozygous50422531
124026480840264809TC14GENICheterozygous50422532
124026541740265418TC21GENICpossibly homozygous50202959