chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
731456263145627GC19GENICpossibly homozygous115546715
731459513145952CT22GENIChomozygous115546717
731461523146153TC26GENIChomozygous115546719
731463293146330CT9GENIChomozygous115546721
731466293146630GA16GENIChomozygous115546723
731488963148897GA9GENIChomozygous115546727
731490423149043AG19GENIChomozygous115546729
731490923149093TC13GENIChomozygous115546731
731516003151601CT6GENIChomozygous116401262
731516133151614GA3GENICheterozygous115546733
731526933152694GA13GENIChomozygous115546735
731532733153274TC4GENIChomozygous115546737
731560083156009CG9GENICheterozygous115546739
731590163159017CT15GENIChomozygous115546741
731623293162330GA30GENIChomozygous115546743
731666613166662GA8GENIChomozygous115546749
731677943167795GA26GENIChomozygous115546751
731680303168031TC28GENIChomozygous115546753