chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136454775136454776GC9GENIChomozygous56941012
4136455016136455017CT16GENIChomozygous56941013
4136455211136455212CT17GENIChomozygous56941014
4136455928136455929CCG18GENIChomozygous56941015
4136461234136461235TC13GENIChomozygous56941017
4136462014136462015AT18GENIChomozygous56941018
4136463389136463390CA18GENIChomozygous56941019
4136464504136464505AT19GENIChomozygous56941021
4136464843136464844AG25GENIChomozygous56941022
4136468054136468055TC12GENIChomozygous56941023
4136468193136468194AG13GENIChomozygous56941024
4136469697136469698GT20GENIChomozygous56941025
4136470136136470149ACCCCAATTGTAT-------------14GENIChomozygous56941026
4136470415136470416CT18GENIChomozygous56941027
4136471761136471762TC14GENIChomozygous56941028
4136473286136473304GTTATATACGTTTCCCTG------------------8GENIChomozygous56941029
4136473779136473780T-7GENIChomozygous56941030
4136474109136474110AG12GENIChomozygous56941031