chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186344807263448072AACA38GENIChomozygous129545553
186344807363448075CT38GENIChomozygous129545554
186345532363455325TG25GENICheterozygous130711006
186345701363457013C44GENIChomozygous129545569
186346659663466596TCTCT25GENICpossibly homozygous130473170
186346785263467852A39GENIChomozygous129545580
186346785763467858T38GENIChomozygous129545581
186346786863467869C38GENIChomozygous129545582
186346788563467886AG38GENIChomozygous110380716
186346788663467887GA38GENIChomozygous119536539
186346789963467899C37GENIChomozygous129545583
186346791463467915A34GENIChomozygous129545584
186346793063467930CA35GENIChomozygous129545585
186347699863476998T1GENIChomozygous129545587
186347700463477004C2GENIChomozygous129545588
186347700763477007G3GENIChomozygous129545589
186347701263477012C4GENIChomozygous129545590
186347701563477016TC7GENIChomozygous129574126
186347701963477020A9GENIChomozygous129545591
186347702963477030C10GENIChomozygous129545592
186347703363477033G11GENIChomozygous129545593
186347704263477043GA11GENIChomozygous119563295
186347705363477054T13GENIChomozygous129545594
186347705763477057A13GENIChomozygous129545595
186347706463477064C14GENIChomozygous129545596
186347707363477074AC17GENIChomozygous119498079
186347707763477077C17GENIChomozygous129545597
186347708163477082CG18GENIChomozygous110921527
186347709763477097A19GENIChomozygous129545598
186347712063477121G19GENIChomozygous129545599
186347712763477128GA19GENIChomozygous110380731
186347713163477131A20GENIChomozygous129545600
186347714863477148C20GENIChomozygous129545601
186347715063477150C19GENIChomozygous129545602
186347716063477161GA17GENIChomozygous119498081
186347717163477171CC13GENIChomozygous129545603
186347717963477180GC13GENIChomozygous119498083
186347719763477199CG14GENIChomozygous130173711
186347720063477201A14GENIChomozygous130173712
186347743563477435C10GENIChomozygous129545604
186348470563484707TT37GENIChomozygous129545614
186348470763484708TG38GENIChomozygous110380765