chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47132091071320911GC32GENIChomozygous112705138
47132109471321095GA25GENIChomozygous112705140
47132120971321210AC33GENIChomozygous112705142
47132128371321284AG30GENIChomozygous112705144
47132132871321329CT17GENIChomozygous112705146
47132133471321335CG16GENIChomozygous112705148
47132140571321406TC26GENIChomozygous112705150
47132147271321473CT26GENIChomozygous112705152
47132154471321545GA34GENICpossibly homozygous112705154
47132160171321602TA30GENIChomozygous112705156
47132167371321674AC20GENIChomozygous112705158
47132175871321759CG27GENIChomozygous112705160
47132184271321843AC27GENIChomozygous112705162
47132202671322027AG24GENIChomozygous112705164
47132233571322336CT21GENIChomozygous112705166
47132259471322595CG15GENIChomozygous112705168
47132306871323069AG26GENIChomozygous112705172
47132315271323153AG23GENIChomozygous112705174
47132346771323468GA34GENIChomozygous112705176
47132362471323625AG26GENIChomozygous112705178
47132391571323916AC6GENIChomozygous112705180
47132395371323954AC8GENIChomozygous112705182
47132399971324000CT10GENIChomozygous112705184
47132414471324145CG14GENIChomozygous112705188
47132430771324308TG32GENIChomozygous112705190
47132434971324350AC30GENIChomozygous112705192
47132444371324444GA30GENIChomozygous112705194
47132458271324583GA20GENIChomozygous112705196
47132498871324989GA25GENIChomozygous112705198