chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162037072620370727CT32GENIChomozygous111752699
162037170220371703GT39GENIChomozygous111752701
162037381420373815CT18GENIChomozygous111752703
162037427620374277AG9GENIChomozygous111752705
162037535920375360CT40GENIChomozygous111752707
162037544020375441TG46GENIChomozygous111752709
162037570020375701CA42GENIChomozygous111752711
162037570220375703GT42GENIChomozygous111752713
162037582720375828AG29GENIChomozygous112130280
162037616020376161TC34GENIChomozygous111752715
162037638620376387AG40GENIChomozygous111752717
162037706920377070GA26GENIChomozygous111752720
162037722720377228TC33GENIChomozygous111752722
162037817320378174GA19GENIChomozygous111752724
162037951120379512CT38GENIChomozygous111752726