chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162037072620370727CT41GENIChomozygous111752699
162037170220371703GT36GENIChomozygous111752701
162037381420373815CT48GENIChomozygous111752703
162037427620374277AG20GENIChomozygous111752705
162037535920375360CT49GENIChomozygous111752707
162037544020375441TG51GENIChomozygous111752709
162037570020375701CA46GENIChomozygous111752711
162037570220375703GT46GENIChomozygous111752713
162037616020376161TC44GENIChomozygous111752715
162037638620376387AG44GENIChomozygous111752717
162037706920377070GA55GENIChomozygous111752720
162037722720377228TC56GENIChomozygous111752722
162037817320378174GA37GENIChomozygous111752724
162037410820374109A42GENIChomozygous129340440
162037582720375828AG36GENIChomozygous112130280
162037951120379512CT40GENIChomozygous111752726
162037989820379898C44GENIChomozygous129340442
162038275120382753GG15GENICheterozygous134030453