chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2184712421184712422GT13GENIChomozygous144612367
2184713275184713276AG16GENIChomozygous144612368
2184713306184713307GA18GENIChomozygous136406275
2184713856184713857GA14GENIChomozygous144612369
2184714176184714177GA15GENIChomozygous142970792
2184714988184714989AG12GENIChomozygous144612370
2184714994184714995TC12GENIChomozygous142970793
2184715378184715379AG9GENIChomozygous142970794
2184715656184715657AG11GENIChomozygous136406278
2184716874184716875TC15GENIChomozygous144612372
2184717043184717044GA15GENICpossibly homozygous144612373
2184720839184720840TG15GENIChomozygous144612374
2184720857184720858AG14GENIChomozygous144612375
2184721291184721292AG13GENIChomozygous144612376
2184721329184721330GT14GENIChomozygous144612377
2184721364184721365AC15GENIChomozygous144612378
2184721458184721459AG13GENIChomozygous144612379
2184722425184722426CA9GENIChomozygous136406280
2184722527184722528AT16GENIChomozygous144612380
2184722712184722713CT16GENIChomozygous144612381
2184722987184722988TC19GENIChomozygous144612382
2184724711184724712AC21GENIChomozygous144612383
2184725323184725324TG19GENIChomozygous144612384
2184726578184726579AT18GENIChomozygous144612385
2184726724184726725AG19GENIChomozygous144612386
2184716668184716669TC19GENICpossibly homozygous141423948
2184722349184722349G4GENIChomozygous144581643
2184728832184728832G18GENIChomozygous135966594
2184729495184729508GCTTGGTTTTTAT15GENIChomozygous144581644
2184731825184731826GA17GENIChomozygous144612387