chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129795360129795361TC20GENIChomozygous574142733
7129795406129795407A-18GENIChomozygous714576945
7129795959129795960TTTGGG8GENIChomozygous714576946
7129795961129795962AATTTAGCTCAGTGGTAGAGCGCTTGCCTAG8GENIChomozygous714576947
7129796093129796094AT16GENIChomozygous574142734
7129796801129796803CC--11GENICheterozygous714576948
7129796802129796803C-11GENICheterozygous714576949
7129797073129797074GA34GENIChomozygous574142735
7129798576129798577AAAAGC16GENIChomozygous714576952
7129798798129798802GAAG----11GENIChomozygous714576954
7129800366129800367T-21GENICpossibly homozygous714576956
7129800826129800827CCAT2GENIChomozygous714576958
7129801566129801568GG--21GENICheterozygous714576959
7129801567129801568G-21GENICpossibly homozygous714576960
7129802532129802533TC25GENIChomozygous574142736
7129803707129803708TA43GENIChomozygous574142737
7129803754129803755AC32GENIChomozygous574142738
7129804462129804465CAC---17GENIChomozygous714576961