chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG26GENIChomozygous942088751
141297497912974980GA25GENIChomozygous942088752
141297572712975728TC20GENIChomozygous942088753
141297600712976008TC20GENIChomozygous942088754
141297603412976035AT26GENIChomozygous942088755
141297709012977091GA5GENIChomozygous942088756
141297778012977781GT30GENIChomozygous942088757
141297853412978535TC21GENIChomozygous942088758
141297897412978975AT38GENIChomozygous942088759
141298059712980598CT15GENIChomozygous942088760
141298061312980614GA14GENIChomozygous942088761
141298103212981033CA24GENIChomozygous942088762
141298248612982487TC21GENIChomozygous942088763
141298580612985807AG18GENIChomozygous942088764
141298595912985960TG27GENIChomozygous942088765
141298615112986152AG21GENIChomozygous942088766
141298684212986843AC20GENIChomozygous942088767
141298761312987614TG20GENIChomozygous942088768
141298766312987664GA24GENIChomozygous942088769
141298792112987922AT17GENIChomozygous942088770
141298835612988357GC17GENIChomozygous942088771
141298866412988665CA16GENIChomozygous942088772
141298876812988769GA35GENIChomozygous942088773
141298877612988777AT36GENIChomozygous942088774
141298889712988898TG25GENIChomozygous942088775
141299108112991082CT12GENIChomozygous942088776
141299289412992895TC30GENIChomozygous942088777
141299407112994072GA37GENIChomozygous942088778
141299411712994118TC43GENIChomozygous942088779
141299423612994237CG30GENIChomozygous942088780
141299473212994733TG26GENIChomozygous942088781