chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121274954712749548CG25GENIChomozygous115362130
121275025012750251AG23GENIChomozygous115259091
121275159012751591TA21GENIChomozygous115362131
121275164812751649GA18GENIChomozygous115362132
121275295012752951GA37GENIChomozygous115259097
121275360212753603GA19GENIChomozygous115362133
121275368912753690GA29GENIChomozygous115362134
121275526512755266GA20GENIChomozygous115362135
121275708512757086TG20GENIChomozygous115259105
121275996012759961CT21GENIChomozygous115467273
121276234912762350CT34GENIChomozygous115362136
121276443812764439CT25GENIChomozygous115362137
121276452312764524CG30GENIChomozygous115362138
121276522212765223AC23GENIChomozygous115259119
121276813512768136AG24GENIChomozygous115259127
121276824412768245TC28GENIChomozygous115259129
121276962312769624CT14GENIChomozygous115362139
121277121912771220GA19GENIChomozygous115362140
121277172412771725GA19GENIChomozygous115362141
121277188512771886TC33GENIChomozygous115362142
121277227912772280CT34GENIChomozygous115467275
121277360712773608CT26GENIChomozygous115259133
121277415612774157TC35GENIChomozygous115259135
121277675912776760TC17GENIChomozygous115362143
121277785712777858GA23GENIChomozygous115259137
121277831712778318GA20GENIChomozygous115416486
121278104912781050CT31GENIChomozygous115362144
121278171812781719AG20GENIChomozygous115259139