chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6146170707146170708AC39GENIChomozygous54766895
6146171618146171619TG39GENICheterozygous55337783
6146172666146172667TC36GENICpossibly homozygous54766896
6146172846146172847CT60GENIChomozygous54766897
6146172924146172925AG44GENIChomozygous54766898
6146173451146173452TC56GENIChomozygous54766899
6146174940146174941TC57GENIChomozygous54766900
6146175399146175400GA31GENICpossibly homozygous54766901
6146176840146176841TC35GENIChomozygous54766902
6146177100146177101GA53GENICpossibly homozygous54766903
6146178635146178636TTG21GENIChomozygous54766904
6146179720146179721GA36GENIChomozygous54766905
6146179848146179849AAAC26GENICheterozygous54766906
6146179960146179966CACACA------19GENICheterozygous54766907
6146181492146181493CT49GENIChomozygous54766908
6146186809146186810AG29GENIChomozygous54766912
6146182124146182125GA43GENICpossibly homozygous54766909
6146182254146182255GC52GENIChomozygous54766910
6146185825146185826AG45GENICpossibly homozygous54766911
6146187581146187582TG42GENICpossibly homozygous54766913