chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136040515860405159TC51GENIChomozygous115070070
136042590860425909G7GENIChomozygous129061245
136042591660425917A10GENIChomozygous129061246
136042592460425925C13GENIChomozygous129061247
136042593360425937CGCG14GENIChomozygous129061248
136042593960425940C14GENIChomozygous129061249
136042597860425978A25GENIChomozygous129061250
136042598860425989G28GENIChomozygous129061251
136042602160426022AG35GENIChomozygous118454921
136042605260426053C39GENIChomozygous130107345
136042590560425906CT5GENIChomozygous115026271
136042595860425959GC19GENIChomozygous115026273
136042600760426008G32GENIChomozygous130107341
136042604260426043C38GENIChomozygous130107342
136042604760426047A40GENIChomozygous130107344
136042606160426062TA37GENIChomozygous118454922
136042606560426066T37GENIChomozygous130107347
136042612060426121T39GENIChomozygous130585350
136042613760426138A37GENIChomozygous132341466
136042614860426148G35GENIChomozygous133016877
136042615160426151T35GENIChomozygous133016878
136042619560426196A6GENIChomozygous130585351
136042620260426202T6GENIChomozygous130585352
136042629560426296GA26GENIChomozygous115026274
136042630460426306GA25GENIChomozygous129061252
136042631360426313A25GENIChomozygous129061253
136042637260426372A14GENIChomozygous129061254
136042638060426380AG14GENIChomozygous129061255
136044508260445082AACAACAAC47GENIChomozygous129061260
136045958160459582TC57GENIChomozygous114365547
136046433060464331CA58GENICpossibly homozygous115070072
136046866860468669TC48GENICpossibly homozygous115070074
136042607960426080TG39GENIChomozygous118592459
136042608060426081GA38GENIChomozygous130422626
136042608760426088C38GENIChomozygous130417952
136042609860426101AAT39GENIChomozygous130417953
136042611560426116G38GENIChomozygous130417954
136042629360426294AG26GENIChomozygous115101002
136043871360438713TA57GENIChomozygous131502782