chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157164737157164738AG15GENIChomozygous114069199
5157165926157165927GA4GENIChomozygous114069201
5157166897157166898GA6GENICheterozygous126206708
5157167999157168000TC10GENIChomozygous114069202
5157168625157168626GA13GENIChomozygous114069203
5157168743157168744AC17GENIChomozygous114069204
5157168821157168822AG20GENIChomozygous114069205
5157169507157169508GA7GENIChomozygous114069206
5157170328157170329CT16GENIChomozygous114069207
5157171391157171392GA19GENIChomozygous114069208
5157171487157171488GA18GENIChomozygous114069209
5157173221157173222TC8GENIChomozygous114069210
5157173437157173438AG11GENIChomozygous114069211
5157175451157175452GA11GENIChomozygous114069212
5157176611157176612GA16GENIChomozygous114069213
5157177470157177471AG9GENIChomozygous114069214
5157179040157179041GA13GENIChomozygous114069215
5157181617157181618GA11GENIChomozygous114069216
5157183146157183147TA6GENIChomozygous114069219
5157186661157186662GA18GENIChomozygous114069220
5157187210157187211GA17GENIChomozygous114069221
5157187320157187321CA15GENIChomozygous114069222
5157187443157187444AG10GENIChomozygous114069223
5157173783157173784AG4GENICheterozygous126313992