chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123747268037472681AG20GENIChomozygous115320480
123747288237472883AG14GENIChomozygous115320482
123747288637472887AG13GENIChomozygous115426324
123747316437473165GA13GENIChomozygous115320484
123747349837473499CT15GENIChomozygous115320486
123747409337474093C13GENICheterozygous131493219
123747411037474110C13GENICheterozygous132167001
123747411137474111C13GENICheterozygous132167002
123747418137474182AT24GENIChomozygous115320488
123747459437474595TC23GENIChomozygous115493837
123747528337475284CT30GENIChomozygous115320490
123747529837475299GC24GENIChomozygous115320492
123747545937475460AG25GENIChomozygous115320494
123747574337475744TC17GENIChomozygous115320496
123747609037476091TC23GENIChomozygous115320498
123747635337476354CT27GENIChomozygous115320502
123747640237476403TG28GENIChomozygous115320504
123747675737476758GA19GENIChomozygous115320506
123747677937476780AG21GENIChomozygous115320508
123747689137476892AG29GENIChomozygous115320510
123747732237477323AG22GENIChomozygous115320512
123747764937477650CA20GENIChomozygous115320514
123747805637478057GC28GENIChomozygous115320516
123747811237478113CG28GENIChomozygous115320518
123747842637478427CG18GENIChomozygous115320520
123747864037478641AG25GENIChomozygous115320522
123747387737473880CCC9GENIChomozygous128985903
123747419237474192T24GENIChomozygous128985904
123747451837474518ACTG15GENIChomozygous128985905
123747597337475973T19GENIChomozygous128985906
123747862037478620C23GENIChomozygous128985909
123747459737474598CG24GENIChomozygous118269728