chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45856614058566141TC38GENIChomozygous57324081
45856624258566243GA29GENIChomozygous57324083
45856627058566271CT30GENIChomozygous56911091
45856640058566401AG27GENIChomozygous57324085
45856649858566499GA40GENIChomozygous56911094
45856667958566680AG45GENICpossibly homozygous56911095
45856690558566906CCA18GENICheterozygous57324087