chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6122250495122250496AG13GENIChomozygous114973359
6122250552122250553TC21GENIChomozygous114973360
6122250910122250911TC24GENIChomozygous114973361
6122251098122251099CG14GENIChomozygous118632043
6122251770122251771GA17GENIChomozygous118632044
6122251792122251793AC19GENIChomozygous118632045
6122251899122251900AG19GENIChomozygous118632046
6122252223122252224TG29GENIChomozygous118632047
6122252281122252282TC25GENIChomozygous118632048
6122252638122252639GC18GENIChomozygous118632049
6122253332122253333CA28GENIChomozygous115162714
6122253381122253382CT21GENIChomozygous115162715
6122254124122254125TC24GENIChomozygous115162718
6122254633122254634TC14GENIChomozygous118632050
6122254650122254651TC13GENIChomozygous118632051
6122254675122254676GA14GENIChomozygous115162720
6122254850122254851GA21GENIChomozygous115162721
6122255315122255316CT30GENIChomozygous118632052
6122255690122255691TC39GENIChomozygous115162724