chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75328787053287871AG20GENIChomozygous822687961
75328803353288034TC11GENIChomozygous822687962
75329103653291037AG16GENIChomozygous822687963
75329106953291070TC15GENIChomozygous822687964
75329479253294793GA18GENIChomozygous822687965
75329593453295935AG18GENIChomozygous822687966
75329678353296784GA12GENIChomozygous822687967
75329863453298635TC19GENIChomozygous822687968
75329914653299147CCAT15GENIChomozygous822687969
75330189053301891GT19GENICpossibly homozygous822687970
75330214353302147AAAT----11GENIChomozygous822687971
75330420853304210TG--9GENIChomozygous822687972
75330426053304261GA12GENIChomozygous822687973
75330675353306754AC9GENIChomozygous822687974
75331001953310020GA21GENIChomozygous822687975
75331184253311843CT14GENIChomozygous822687976
75331193753311938AG10GENIChomozygous822687977
75331274953312750CT23GENIChomozygous822687978
75331327453313275CG12GENIChomozygous822687979
75331350753313508TTGC9GENIChomozygous822687980
75331615853316159AG11GENIChomozygous822687981
75331757953317580T-16GENIChomozygous822687982
75331822053318221GT8GENIChomozygous822687983
75331866753318668TA17GENIChomozygous822687984
75332215353322154GA15GENIChomozygous822687985
75332221953322220CT12GENIChomozygous822687986
75332223053322231GA12GENIChomozygous822687987
75332236453322365GA17GENIChomozygous822687988
75332241153322412TA17GENIChomozygous822687989
75332355653323557CA13GENIChomozygous822687990
75332483553324836GA20GENIChomozygous822687991
75332514953325150CCCCT11GENIChomozygous822687992
75332560753325608AG9GENIChomozygous822687993
75332727053327271GA31GENIChomozygous822687994