chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG37GENIChomozygous112858184
4140887405140887406GC28GENIChomozygous112858186
4140887526140887527AG19GENIChomozygous112858188
4140887695140887696GA26GENIChomozygous113175920
4140888161140888162GT19GENIChomozygous113175922
4140894149140894150GA22GENIChomozygous112858194
4140896988140896989GA32GENIChomozygous112858196
4140897414140897415CT18GENIChomozygous113175926
4140902715140902716TC16GENIChomozygous112858204
4140902957140902958AG22GENIChomozygous112858206
4140903807140903808CT21GENIChomozygous112858210
4140906350140906351AG31GENIChomozygous113175928
4140906395140906396AG40GENIChomozygous112858212
4140907673140907674TC23GENICheterozygous113057533
4140908274140908275TG18GENIChomozygous112858214
4140908798140908799AG40GENIChomozygous113175930
4140908994140908995GC15GENIChomozygous113057535
4140909196140909197CT31GENIChomozygous112858220
4140909244140909245GT25GENIChomozygous112858222
4140909248140909249TA25GENIChomozygous112858224
4140916630140916631TG20GENIChomozygous112858250
4140916631140916632CA19GENIChomozygous112858252
4140916796140916797CG22GENIChomozygous112858254