chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136454775136454776GC5GENIChomozygous56941012
4136455016136455017CT33GENIChomozygous56941013
4136455211136455212CT32GENIChomozygous56941014
4136455928136455929CCG42GENIChomozygous56941015
4136460450136460451GA16GENIChomozygous56941016
4136461234136461235TC31GENIChomozygous56941017
4136462014136462015AT29GENIChomozygous56941018
4136463389136463390CA41GENIChomozygous56941019
4136463552136463553A-26GENICpossibly homozygous57339372
4136463751136463755GGGT----3GENICheterozygous58338787
4136464504136464505AT33GENIChomozygous56941021
4136464843136464844AG32GENIChomozygous56941022
4136468054136468055TC37GENIChomozygous56941023
4136468193136468194AG32GENIChomozygous56941024
4136469697136469698GT38GENIChomozygous56941025
4136470136136470149ACCCCAATTGTAT-------------39GENIChomozygous56941026
4136470415136470416CT29GENIChomozygous56941027
4136471761136471762TC29GENIChomozygous56941028
4136473286136473304GTTATATACGTTTCCCTG------------------31GENIChomozygous56941029
4136473779136473780T-27GENIChomozygous56941030
4136474109136474110AG31GENIChomozygous56941031