chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146262818462628185CT7GENIChomozygous113822234
146262848262628483CA17GENIChomozygous113822236
146262850962628510AG21GENIChomozygous113479123
146263000262630003TC9GENIChomozygous113479126
146263147262631473CA12GENIChomozygous113822244
146263032562630326GA32GENIChomozygous113822238
146263057262630573GT28GENIChomozygous113822240
146263058262630583GA28GENIChomozygous113822242
146263152762631528CA14GENIChomozygous113822246
146263200562632006TC41GENIChomozygous113822248
146263251362632514TC19GENIChomozygous113822250
146263273462632735GC27GENIChomozygous113822252
146263367262633673CG18GENIChomozygous113479136
146263367962633680TC19GENIChomozygous113822254
146263462862634629TC12GENIChomozygous113479137
146263527262635273TA20GENIChomozygous113822256
146263764962637650TC41GENIChomozygous113479140
146263826762638268GA13GENICpossibly homozygous113822258
146263891662638917GA27GENIChomozygous113479142
146264128462641285TA9GENIChomozygous113479143
146264302962643030TC19GENIChomozygous113479144
146264317962643180AG21GENIChomozygous113479145
146264354562643546AG20GENIChomozygous113479146
146264415162644152CT9GENIChomozygous113479147
146264477962644780CT15GENIChomozygous113822260
146264544062645441CG14GENIChomozygous113479148
146264560362645604AG23GENIChomozygous113479149
146263453462634535CT7GENIChomozygous113678003