chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136454775136454776GC7GENIChomozygous56941012
4136455016136455017CT18GENICpossibly homozygous56941013
4136455211136455212CT17GENIChomozygous56941014
4136455928136455929CCG22GENIChomozygous56941015
4136461234136461235TC21GENIChomozygous56941017
4136462014136462015AT20GENIChomozygous56941018
4136463389136463390CA24GENIChomozygous56941019
4136463552136463553A-3GENICheterozygous57339372
4136464504136464505AT9GENICheterozygous56941021
4136464843136464844AG19GENICpossibly homozygous56941022
4136468054136468055TC21GENIChomozygous56941023
4136468193136468194AG25GENICpossibly homozygous56941024
4136469697136469698GT2GENIChomozygous56941025
4136470136136470149ACCCCAATTGTAT-------------4GENICheterozygous56941026
4136470415136470416CT13GENIChomozygous56941027
4136471761136471762TC9GENIChomozygous56941028
4136473779136473780T-10GENIChomozygous56941030
4136474109136474110AG31GENIChomozygous56941031