chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157164737157164738AG45GENIChomozygous114069199
5157165903157165904GT49GENICpossibly homozygous114069200
5157165926157165927GA52GENIChomozygous114069201
5157167999157168000TC61GENIChomozygous114069202
5157168625157168626GA67GENIChomozygous114069203
5157168743157168744AC57GENIChomozygous114069204
5157168821157168822AG59GENIChomozygous114069205
5157169507157169508GA59GENIChomozygous114069206
5157170328157170329CT36GENICpossibly homozygous114069207
5157171391157171392GA42GENIChomozygous114069208
5157171487157171488GA52GENICpossibly homozygous114069209
5157173221157173222TC53GENIChomozygous114069210
5157173437157173438AG57GENICpossibly homozygous114069211
5157175451157175452GA42GENIChomozygous114069212
5157176611157176612GA54GENIChomozygous114069213
5157177470157177471AG52GENIChomozygous114069214
5157179040157179041GA56GENIChomozygous114069215
5157181617157181618GA46GENICpossibly homozygous114069216
5157182451157182452GA17GENICheterozygous114069217
5157182706157182707GA19GENICheterozygous114069218
5157183146157183147TA68GENIChomozygous114069219
5157186661157186662GA46GENICpossibly homozygous114069220
5157187210157187211GA47GENIChomozygous114069221
5157187320157187321CA54GENIChomozygous114069222
5157187443157187444AG32GENICpossibly homozygous114069223