chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47898223078982231AT36GENICpossibly homozygous112740109
47898230678982307CT50GENIChomozygous112740111
47898366778983668CT52GENIChomozygous112740113
47898527978985280AG29GENIChomozygous112740115
47898900378989004TC55GENIChomozygous112740117
47899068378990684GA40GENIChomozygous112740119
47899116278991163AG27GENIChomozygous112740121
47899141578991416CT54GENIChomozygous112740123
47899283678992837CG62GENIChomozygous112740125
47899321478993215TC36GENIChomozygous112740127
47899366078993661GA25GENIChomozygous112740129
47899436578994366AC54GENIChomozygous112740131
47899478278994783GC19GENIChomozygous112740133
47899536778995368CT49GENIChomozygous112740135
47899543878995439AG49GENIChomozygous112740137
47899641178996412AT43GENIChomozygous112740139
47899785478997855CT35GENIChomozygous112740141
47899834878998349CT23GENIChomozygous112740143
47900252979002530GA26GENIChomozygous112740145
47900274379002744CT9GENIChomozygous112740147