chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107371510107371511CT22GENIChomozygous72445054
3107371713107371714CT15GENIChomozygous72074328
3107372857107372858TC27GENIChomozygous72074338
3107374964107374965TC41GENIChomozygous72074344
3107381199107381200CT8GENIChomozygous72074352
3107382345107382346GT7GENIChomozygous72074364
3107384188107384189TC29INTERGENIChomozygous72074386
3107388930107388931CT3INTERGENIChomozygous72445061
3107391156107391157GA11INTERGENIChomozygous72445064
3107398010107398011CA21INTERGENIChomozygous72445067
3107401656107401657CT3INTERGENIChomozygous79687512
3107401662107401663TC3INTERGENIChomozygous72445070
3107402129107402130AG22GENIChomozygous72074442
3107405853107405854AC27GENIChomozygous72445082
3107411181107411182GA25GENIChomozygous72074462
3107412950107412951TA12GENIChomozygous72445086
3107415216107415217CG18GENIChomozygous72445089
3107415483107415484AG27GENIChomozygous72074478
3107416120107416121CA10GENIChomozygous72074484
3107416304107416305AT22GENICpossibly homozygous72445092
3107416315107416316AG23GENICheterozygous72445095
3107401657107401658TA3INTERGENIChomozygous74950476