chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157164737157164738AG35GENIChomozygous114069199
5157165903157165904GT14GENIChomozygous114069200
5157165926157165927GA18GENIChomozygous114069201
5157167999157168000TC28GENIChomozygous114069202
5157168625157168626GA31GENIChomozygous114069203
5157168743157168744AC35GENIChomozygous114069204
5157168821157168822AG34GENIChomozygous114069205
5157169507157169508GA36GENIChomozygous114069206
5157170328157170329CT24GENIChomozygous114069207
5157171391157171392GA21GENIChomozygous114069208
5157171487157171488GA20GENIChomozygous114069209
5157173221157173222TC35GENIChomozygous114069210
5157173437157173438AG38GENIChomozygous114069211
5157175451157175452GA26GENIChomozygous114069212
5157176611157176612GA23GENIChomozygous114069213
5157177470157177471AG37GENIChomozygous114069214
5157179040157179041GA26GENIChomozygous114069215
5157181617157181618GA18GENIChomozygous114069216
5157183146157183147TA25GENIChomozygous114069219
5157186661157186662GA22GENIChomozygous114069220
5157187210157187211GA22GENIChomozygous114069221
5157187320157187321CA35GENIChomozygous114069222