chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153667978436679785CT30GENIChomozygous49360289
153668018536680186AG27GENIChomozygous49360290
153668222836682229CT38GENIChomozygous49360291
153668270036682701AT32GENIChomozygous49360292
153668274836682749GGCA15GENICheterozygous49360293
153668277536682776CCAT31GENICpossibly homozygous49360294
153668526436685265AC37GENIChomozygous48499128
153668568436685685TC22GENIChomozygous49360295
153668614736686148TC36GENIChomozygous48499130
153668532036685321G-19GENIChomozygous48282322
153668534936685351CA--33GENIChomozygous48282323
153668536536685366GT32GENIChomozygous48282324
153668658436686585GGTTTTTTTTT15GENIChomozygous49148545
153668658636686587CCT11GENICheterozygous49048431
153668675936686761GA--28GENIChomozygous48282329
153668676536686766A-28GENIChomozygous48282330
153668677036686771G-29GENIChomozygous48282331
153668677636686777A-25GENIChomozygous48282332
153668679936686800A-30GENIChomozygous48282333
153668680436686805A-34GENIChomozygous48282334
153668681136686812A-30GENIChomozygous48282335
153668939536689396GA32GENIChomozygous48499139
153669006736690068TTAA31GENIChomozygous49360296
153669097836690981AAA---15GENICpossibly homozygous49360297
153669098036690981A-15GENICheterozygous49048437
153669107136691072CT38GENIChomozygous49360298
153669348136693484AAG---16GENICheterozygous49360299
153669417736694178AG22GENIChomozygous49360300
153669437436694375AG12GENIChomozygous49360301
153669457736694578CT32GENIChomozygous49360302
153669508436695085GA35GENIChomozygous49360303
153669566336695664TC16GENIChomozygous49360304
153669667636696677CA21GENIChomozygous49360305
153669698636696987A-16GENICpossibly homozygous49187363
153669700036697001A-19GENICheterozygous49326508
153669751136697515AGGG----17GENIChomozygous49360306
153669820836698209GA28GENIChomozygous49360307