chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257455055257455055ACTC19GENIChomozygous127768551
2257455309257455309C11GENICpossibly homozygous132022219
2257455848257455853TATGA27GENIChomozygous132022220
2257457070257457071AT21GENIChomozygous110411982
2257459373257459374CT19GENIChomozygous110411988
2257460347257460355GAGAATTT22GENIChomozygous132022221
2257462199257462200AG22GENIChomozygous111043678
2257477585257477586GA17GENIChomozygous111043680
2257480123257480124AG18GENIChomozygous110412010
2257480136257480137TA16GENIChomozygous111043682
2257480886257480887AG24GENIChomozygous110412012
2257481191257481192A13GENICheterozygous127768560