chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124686255146862552GC23GENIChomozygous50221100
124686274046862741GA17GENIChomozygous50342258
124686573046865731TC7GENIChomozygous50221147
124686609746866098AAG5GENICheterozygous50221150
124686621246866213TC12GENICheterozygous50221156
124686645446866455TC5GENICheterozygous50221158
124686661546866616AACCCC1GENIChomozygous50342261
124686687546866876TTTC10GENIChomozygous50342265
124686695546866956CT4GENIChomozygous50221169
124686720946867210TC5GENIChomozygous50221171
124686869546868696TC5GENICheterozygous50221186
124686908146869082CT9GENIChomozygous50342269
124686908346869084CT9GENIChomozygous50342271
124686919846869199AG1GENIChomozygous50221190
124686988446869885A-3GENICheterozygous50342273
124687009846870099TC12GENIChomozygous50221196
124687023546870236CG13GENICpossibly homozygous50221198
124687036646870367CCG16GENICpossibly homozygous50342277
124687049246870493TG16GENICpossibly homozygous50221202
124687072346870735TGTGTGCGTGCA------------4GENICheterozygous50513420
124687215246872153CT13GENIChomozygous50342279
124687240046872401TTG1GENIChomozygous50221230
124687304546873046GA13GENICheterozygous50342281
124687312846873129GA24GENIChomozygous50342283
124687331546873316AG24GENICpossibly homozygous50221238
124687347746873478CT14GENIChomozygous50221239
124687514246875143AC15GENIChomozygous50221247
124687518246875183CT22GENIChomozygous50342287
124687542746875428CT9GENIChomozygous50342289
124687642746876432GCCCC-----3GENICheterozygous50221257