chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46856957068569571GA35GENIChomozygous112691587
46857027568570276AG23GENIChomozygous112691589
46857128068571281AG32GENIChomozygous112691591
46857142268571423TC43GENIChomozygous112691593
46857193368571934CT37GENIChomozygous113347162
46857397968573980TA20GENIChomozygous112691601
46857470268574703CT31GENIChomozygous112691603
46857751768577518AG27GENIChomozygous112691607
46857808468578085GA39GENIChomozygous112691611
46857927268579273GA16GENIChomozygous112691613
46857951868579519AG37GENIChomozygous112691615
46858057768580578CT26GENIChomozygous112691617
46858124168581242TA31GENIChomozygous112691619
46858274268582743CG17GENIChomozygous112691621
46858354968583550TC29GENIChomozygous112691623
46858361868583619CT21GENIChomozygous112691625
46858568468585685TC25GENIChomozygous112691627
46858795168587952AG20GENICpossibly homozygous112691629
46859278668592787TC32GENIChomozygous112691633