chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43461493034614931CT12GENIChomozygous640770863
43461708234617083TC13GENIChomozygous640770864
43461781934617820TC20GENIChomozygous640770865
43461803834618039TC17GENIChomozygous640770866
43461913934619140GA21GENIChomozygous640770867
43461947634619477GT14GENIChomozygous640770868
43462030134620302AG15GENIChomozygous640770869
43462032134620322CT12GENIChomozygous640770870
43462048134620482CT24GENIChomozygous640770871
43462055134620552TA23GENIChomozygous640770872
43462070434620705GA12GENIChomozygous640770873
43462070934620710CA12GENIChomozygous640770874
43462073734620738CT9GENIChomozygous640770875
43462114734621148AG9GENICpossibly homozygous640770876
43462115234621155AAA---9GENICpossibly homozygous751489650
43462131434621315GT26GENIChomozygous640770877
43462151934621520GGA15GENIChomozygous751489651
43462189634621897TC18GENIChomozygous640770878
43462243834622439CT21GENIChomozygous640770879
43462271834622719TTTG21GENIChomozygous751489653
43462276834622769GA24GENIChomozygous640770880
43462291534622916TC16GENIChomozygous640770881
43462301234623016ACAC----11GENICheterozygous751489655
43462301434623016AC--11GENICheterozygous751489656
43462308234623083A-15GENIChomozygous751489657
43462309034623091GA17GENIChomozygous640770882
43462356534623566AG20GENIChomozygous640770883
43462403534624036GA17GENIChomozygous640770884
43462423234624233TC22GENIChomozygous640770885