chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124686255146862552GC22GENIChomozygous50221100
124686274046862741GA21GENIChomozygous50342258
124686573046865731TC6GENIChomozygous50221147
124686609746866098AAG9GENICheterozygous50221150
124686621246866213TC23GENIChomozygous50221156
124686645446866455TC11GENIChomozygous50221158
124686661546866616AACCCC5GENIChomozygous50342261
124686687546866876TTTC14GENICpossibly homozygous50342265
124686695546866956CT20GENIChomozygous50221169
124686720946867210TC20GENIChomozygous50221171
124686722846867229T-13GENICheterozygous50545792
124686825146868254TTT---13GENIChomozygous50342267
124686869546868696TC18GENIChomozygous50221186
124686908146869082CT12GENIChomozygous50342269
124686908346869084CT13GENIChomozygous50342271
124686919846869199AG13GENIChomozygous50221190
124686988446869885A-14GENIChomozygous50342273
124686998646869987GGTTTT7GENIChomozygous50342275
124687009846870099TC13GENIChomozygous50221196
124687023546870236CG23GENIChomozygous50221198
124687036646870367CCG26GENIChomozygous50342277
124687049246870493TG14GENIChomozygous50221202
124687072346870735TGTGTGCGTGCA------------20GENIChomozygous50513420
124687215246872153CT19GENIChomozygous50342279
124687240046872401TTG5GENIChomozygous50221230
124687304546873046GA33GENICpossibly homozygous50342281
124687312846873129GA19GENIChomozygous50342283
124687331546873316AG21GENIChomozygous50221238
124687347746873478CT28GENIChomozygous50221239
124687370746873708AATGTGTGTG16GENIChomozygous50342285
124687490746874917AAACCAAACC----------7GENIChomozygous50545794
124687514246875143AC22GENIChomozygous50221247
124687518246875183CT25GENIChomozygous50342287
124687524446875245TTTGTGTG9GENICheterozygous50221249
124687524446875245TTTGTGTGTG9GENICheterozygous50545795
124687524446875245TTTGTGTGTGTG9GENICheterozygous50559279
124687527246875273CCTGTG6GENIChomozygous50545797
124687542746875428CT24GENIChomozygous50342289
124687642746876432GCCCC-----3GENIChomozygous50221257