chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144746069144746070AG43GENIChomozygous114037693
5144746504144746505TC42GENIChomozygous114037694
5144747086144747087GA63GENIChomozygous114037697
5144748059144748060GC44GENIChomozygous114037699
5144749663144749664CA10GENIChomozygous118846277
5144749895144749896AT38GENIChomozygous114037700
5144750770144750771AG42GENICpossibly homozygous114037701
5144751018144751019TC43GENIChomozygous114037702
5144751168144751169AC50GENIChomozygous114037703
5144752985144752986CT59GENIChomozygous114037707
5144753208144753209CT44GENIChomozygous114037708
5144755220144755221TC36GENIChomozygous114037709
5144755301144755302CT58GENIChomozygous114037710
5144755308144755309GA60GENIChomozygous114037711
5144756106144756107GA40GENIChomozygous114037712
5144756384144756385GC20GENIChomozygous118846278
5144756386144756387GC20GENIChomozygous118846280
5144757963144757964TG42GENIChomozygous114037713
5144758049144758050AG40GENIChomozygous114037714
5144758266144758267CT36GENIChomozygous114037715
5144758311144758312GT37GENIChomozygous118846282
5144759427144759428CT26GENIChomozygous114037720
5144759469144759470AC35GENIChomozygous114037721
5144760334144760335AT44GENIChomozygous114037722
5144760661144760662GA44GENIChomozygous114037723