chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162037072620370727CT20GENIChomozygous111752699
162037170220371703GT15GENICpossibly homozygous111752701
162037381420373815CT20GENIChomozygous111752703
162037427620374277AG7GENIChomozygous111752705
162037535920375360CT21GENIChomozygous111752707
162037544020375441TG23GENIChomozygous111752709
162037570020375701CA17GENIChomozygous111752711
162037570220375703GT16GENIChomozygous111752713
162037616020376161TC24GENIChomozygous111752715
162037638620376387AG16GENIChomozygous111752717
162037706920377070GA23GENIChomozygous111752720
162037722720377228TC14GENIChomozygous111752722
162037817320378174GA21GENIChomozygous111752724
162037951120379512CT15GENIChomozygous111752726
162037989820379898C17GENIChomozygous129340442
162037410820374109A17GENIChomozygous129340440
162037582720375828AG13GENIChomozygous112130280