chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134259540542595406GT19GENIChomozygous144929401
134259592642595927CA20GENIChomozygous144929402
134259633642596337TC16GENIChomozygous144929403
134259639042596390GG17GENIChomozygous144924659
134259647442596475AT20GENIChomozygous143578674
134259679942596800G14GENIChomozygous144924660
134259680342596806GGG14GENIChomozygous144924661
134259683642596837TC14GENIChomozygous144929404
134259704742597048TC18GENIChomozygous144929405
134259728142597282TC17GENIChomozygous144929406
134259730442597305CT14GENIChomozygous144929407
134259738342597384GC5GENIChomozygous144929408
134259751442597515CT10GENIChomozygous144929409
134259831242598312CC10GENIChomozygous144924662
134259835842598362TCCA7GENIChomozygous144924663
134259851042598511TC8GENIChomozygous144929410
134259878442598785TA16GENIChomozygous143578679
134259878742598837CTTTTCTTTCCGTCAAGACCTTATCTGCACTCTCTGCAAATTAAGTCCTA17GENIChomozygous143549449
134259913542599136TC23GENIChomozygous143578680
134259939442599395CT17GENIChomozygous143578681
134260009342600094AG21GENIChomozygous144929411
134260011642600117GA19GENIChomozygous144929412
134260021042600211TC15GENIChomozygous144929413
134260068942600690AG9GENIChomozygous143578683
134260073142600732CT16GENIChomozygous143578684
134260092742600928CA20GENIChomozygous143578685
134260098442600985GA18GENIChomozygous144929414
134260104142601042CG17GENIChomozygous144929415
134260107142601072C15GENIChomozygous144924664
134260239842602399CT17GENIChomozygous144929416
134260250142602501TG17GENIChomozygous144924665
134260261942602620C11GENIChomozygous143549450
134260298442602985AG22GENIChomozygous143578693
134260305642603057GA17GENIChomozygous144929417
134260340642603407A14GENIChomozygous144924666
134260353142603532AG21GENIChomozygous144929418
134260356842603569CG23GENIChomozygous144929419
134260419042604191CT21GENICpossibly homozygous144929420
134259879742598798CA17GENICheterozygous403337474
134259879742598798C17GENIChomozygous403337473