chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107371510107371511CT12GENIChomozygous72445054
3107371713107371714CT8GENIChomozygous72074328
3107372857107372858TC29GENIChomozygous72074338
3107374964107374965TC24GENIChomozygous72074344
3107381199107381200CT10GENIChomozygous72074352
3107382345107382346GT20GENICpossibly homozygous72074364
3107384188107384189TC36INTERGENIChomozygous72074386
3107391156107391157GA12INTERGENICheterozygous72445064
3107391710107391711CG33INTERGENICheterozygous72074406
3107398010107398011CA14INTERGENIChomozygous72445067
3107401662107401663TC3INTERGENIChomozygous72445070
3107401656107401657CT4INTERGENIChomozygous79687512
3107401657107401658TA3INTERGENIChomozygous74950476
3107402129107402130AG14GENIChomozygous72074442
3107405853107405854AC36GENIChomozygous72445082
3107411181107411182GA46GENIChomozygous72074462
3107412950107412951TA27GENIChomozygous72445086
3107415216107415217CG35GENIChomozygous72445089
3107415483107415484AG33GENIChomozygous72074478
3107416120107416121CA19GENIChomozygous72074484
3107416304107416305AT23GENICpossibly homozygous72445092
3107416315107416316AG22GENICheterozygous72445095