chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2114745357114745358CT9GENIChomozygous580725820
2114745405114745406AG35GENIChomozygous579559548
2114745513114745514CT29GENICpossibly homozygous579559549
2114745930114745931TC12GENICpossibly homozygous579559550
2114745953114745954TC6GENICheterozygous579559551
2114747143114747144TA6GENIChomozygous579559552
2114747169114747172TTT---1GENIChomozygous717361124
2114747537114747538CT21GENICpossibly homozygous579559553
2114747680114747681GA17GENICpossibly homozygous579559554
2114748669114748670CT18GENICpossibly homozygous580725821
2114749309114749310TA25GENICpossibly homozygous579559555
2114749643114749644AG4GENIChomozygous579559556
2114750211114750212TG34GENIChomozygous579559557
2114750661114750662AC18GENICpossibly homozygous579559558
2114750738114750739AC9GENICpossibly homozygous579559559
2114750739114750740GA10GENICpossibly homozygous580725822
2114750940114750941AG19GENIChomozygous579559560
2114751124114751125CT34GENICpossibly homozygous579559561
2114751682114751683TC15GENIChomozygous579559562
2114751777114751778CG20GENICpossibly homozygous579559563
2114752163114752164AG19GENIChomozygous579559564
2114752297114752298AG11GENICpossibly homozygous579559565
2114752355114752356CG17GENIChomozygous579559566
2114752802114752803TC12GENIChomozygous579559567
2114753270114753271TC12GENIChomozygous579559568
2114753307114753308CG9GENICheterozygous579559569
2114753354114753355CT20GENIChomozygous579559570
2114753694114753695CT10GENIChomozygous579559571