chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146262818462628185CT21GENIChomozygous113822234
146262848262628483CA22GENIChomozygous113822236
146263000262630003TC23GENIChomozygous113479126
146262850962628510AG20GENIChomozygous113479123
146263032562630326GA16GENIChomozygous113822238
146263057262630573GT24GENIChomozygous113822240
146263058262630583GA24GENIChomozygous113822242
146263147262631473CA12GENIChomozygous113822244
146263152762631528CA15GENIChomozygous113822246
146263200562632006TC11GENIChomozygous113822248
146263251362632514TC24GENIChomozygous113822250
146263273462632735GC30GENIChomozygous113822252
146263367262633673CG14GENIChomozygous113479136
146263411662634118AC15GENIChomozygous129166896
146263442762634427A18GENIChomozygous129166897
146263453462634535CT23GENIChomozygous113678003
146263367962633680TC13GENIChomozygous113822254
146263462862634629TC25GENIChomozygous113479137
146263527262635273TA20GENIChomozygous113822256
146263532462635325AG17GENIChomozygous113479138
146263532662635331GAATG17GENIChomozygous129166898
146263533362635333GTCG17GENIChomozygous129166899
146263764962637650TC19GENIChomozygous113479140
146263826762638268GA30GENIChomozygous113822258
146263891662638917GA25GENIChomozygous113479142
146263979762639797A21GENICpossibly homozygous129166900
146264128462641285TA18GENIChomozygous113479143
146264302962643030TC22GENIChomozygous113479144
146264317962643180AG27GENIChomozygous113479145
146264354562643546AG23GENIChomozygous113479146
146264415162644152CT12GENIChomozygous113479147
146264477962644780CT14GENIChomozygous113822260
146264544062645441CG15GENIChomozygous113479148
146264560362645604AG25GENIChomozygous113479149