chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5168050762168050763CT28GENIChomozygous80842045
5168051907168051908TC21GENIChomozygous71525763
5168052004168052005TA22GENIChomozygous71525766
5168052353168052354TC36GENIChomozygous71201029
5168052890168052891GA22GENIChomozygous72472471
5168053253168053254GA30GENICpossibly homozygous72472474
5168053383168053384AG27GENIChomozygous71201031
5168054416168054417AG31GENIChomozygous73421414
5168055114168055115TC21GENIChomozygous80842046
5168055895168055896GT33GENIChomozygous80842047
5168056870168056871CT17GENIChomozygous71201039
5168056999168057000AG27GENIChomozygous80842048
5168057134168057135TC32GENIChomozygous71201041
5168057181168057182TC41GENIChomozygous71201043
5168060141168060142CA29GENIChomozygous80842052
5168057982168057983GA29GENIChomozygous80842049
5168058630168058631GA36GENIChomozygous72472501
5168059515168059516AC23GENIChomozygous80842050
5168059732168059733CG27GENIChomozygous80842051
5168061396168061397AT24GENIChomozygous71525775