chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG11GENIChomozygous948052661
141297519412975195AG23GENIChomozygous948052662
141297572712975728TC25GENIChomozygous948052663
141297600712976008TC32GENIChomozygous948052664
141297603412976035AT25GENIChomozygous948052665
141297709012977091GA3GENIChomozygous948052666
141297859112978592CT5GENIChomozygous948052667
141297897412978975AT27GENIChomozygous948052668
141297912512979126GT29GENIChomozygous948052669
141298061312980614GA37GENIChomozygous948052670
141298096712980968GA18GENIChomozygous948052671
141298248612982487TC23GENIChomozygous948052672
141298580612985807AG38GENIChomozygous948052673
141298595912985960TG28GENIChomozygous948052674
141298767512987676AG18GENIChomozygous948052675
141298792112987922AT18GENIChomozygous948052676
141298835612988357GC24GENIChomozygous948052677
141298846512988466TG10GENIChomozygous948052678
141298866412988665CA10GENIChomozygous948052679
141298876812988769GA28GENIChomozygous948052680
141298877612988777AT26GENIChomozygous948052681
141298885412988855TG18GENIChomozygous948052682
141298889712988898TG23GENIChomozygous948052683
141298932912989330GA23GENIChomozygous948052684
141298998812989989AT5GENIChomozygous948052685
141299016312990164TA26GENIChomozygous948052686
141299411712994118TC15GENIChomozygous948052687
141299423612994237CG11GENIChomozygous948052688