chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2114745357114745358CT8GENIChomozygous59030744
2114745405114745406AG16GENIChomozygous59030745
2114745513114745514CT19GENIChomozygous59030746
2114745930114745931TC12GENIChomozygous59030747
2114745953114745954TC9GENIChomozygous59030748
2114747143114747144TA18GENIChomozygous59030749
2114747169114747172TTT---17GENICpossibly homozygous59030750
2114747171114747172T-17GENICheterozygous60574734
2114747537114747538CT27GENIChomozygous59030751
2114747680114747681GA23GENIChomozygous59030752
2114748669114748670CT15GENIChomozygous59030753
2114749309114749310TA18GENIChomozygous59030754
2114749643114749644AG11GENIChomozygous59030755
2114750211114750212TG14GENIChomozygous59030756
2114750661114750662AC20GENIChomozygous59030757
2114750738114750739AC13GENIChomozygous60449339
2114750739114750740GA13GENIChomozygous60449340
2114750940114750941AG16GENIChomozygous59030758
2114751124114751125CT26GENIChomozygous59030759
2114751682114751683TC16GENIChomozygous59030760
2114751777114751778CG15GENIChomozygous59030761
2114752163114752164AG14GENIChomozygous59030762
2114752297114752298AG11GENIChomozygous59030763
2114752355114752356CG13GENIChomozygous59030764
2114752802114752803TC10GENIChomozygous59030765
2114753270114753271TC26GENIChomozygous59030766
2114753307114753308CG17GENIChomozygous59030767
2114753354114753355CT7GENIChomozygous59030768
2114753694114753695CT11GENIChomozygous59030769