chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2184712421184712422GT47GENIChomozygous144612367
2184713275184713276AG48GENIChomozygous144612368
2184713306184713307GA43GENIChomozygous136406275
2184713856184713857GA31GENIChomozygous144612369
2184714176184714177GA49GENIChomozygous142970792
2184714988184714989AG42GENIChomozygous144612370
2184714994184714995TC41GENIChomozygous142970793
2184715362184715363CT35GENIChomozygous144612371
2184715378184715379AG35GENIChomozygous142970794
2184715656184715657AG38GENIChomozygous136406278
2184716874184716875TC35GENIChomozygous144612372
2184717043184717044GA46GENIChomozygous144612373
2184720839184720840TG33GENIChomozygous144612374
2184720857184720858AG38GENIChomozygous144612375
2184721291184721292AG32GENIChomozygous144612376
2184721329184721330GT36GENIChomozygous144612377
2184721364184721365AC36GENICpossibly homozygous144612378
2184721458184721459AG24GENIChomozygous144612379
2184722425184722426CA15GENIChomozygous136406280
2184722527184722528AT28GENIChomozygous144612380
2184722712184722713CT34GENIChomozygous144612381
2184722987184722988TC41GENIChomozygous144612382
2184724711184724712AC48GENICpossibly homozygous144612383
2184725323184725324TG43GENIChomozygous144612384
2184726578184726579AT37GENIChomozygous144612385
2184726724184726725AG34GENIChomozygous144612386
2184728832184728832G49GENIChomozygous135966594
2184716668184716669TC55GENIChomozygous141423948
2184722349184722349G9GENIChomozygous144581643
2184729495184729508GCTTGGTTTTTAT40GENIChomozygous144581644
2184731825184731826GA30GENIChomozygous144612387