chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45856614058566141TC19GENIChomozygous57324081
45856624258566243GA26GENIChomozygous57324083
45856627058566271CT19GENIChomozygous56911091
45856640058566401AG29GENIChomozygous57324085
45856649858566499GA31GENIChomozygous56911094
45856667958566680AG29GENIChomozygous56911095
45856690558566906CCA15GENICpossibly homozygous57324087