chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55900828059008281CG22GENICpossibly homozygous113819992
55900984559009846TC59GENIChomozygous113819994
55901015359010154CT49GENIChomozygous113819996
55901043959010440CT40GENIChomozygous113819998
55901130659011307GA66GENIChomozygous113820000
55901179159011792GA31GENIChomozygous113820002
55901311659013117AT31GENIChomozygous113820004
55901333759013338GA59GENIChomozygous113820006
55901353759013538GC58GENIChomozygous113820008
55901385559013856CT60GENIChomozygous113820010
55901444959014450AG50GENIChomozygous113820012
55901516159015162CT44GENIChomozygous113820014