chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124686255146862552GC34GENIChomozygous50221100
124686274046862741GA21GENIChomozygous50342258
124686573046865731TC11GENIChomozygous50221147
124686609746866098AAG15GENIChomozygous50221150
124686621246866213TC17GENIChomozygous50221156
124686645446866455TC20GENIChomozygous50221158
124686661546866616AACCCC5GENIChomozygous50342261
124686687546866876TTTC7GENIChomozygous50342265
124686695546866956CT9GENIChomozygous50221169
124686720946867210TC14GENIChomozygous50221171
124686825146868254TTT---16GENICpossibly homozygous50342267
124686869546868696TC13GENIChomozygous50221186
124686908146869082CT12GENIChomozygous50342269
124686908346869084CT12GENIChomozygous50342271
124686919846869199AG14GENIChomozygous50221190
124686988446869885A-17GENIChomozygous50342273
124686998646869987GGTTTT10GENICpossibly homozygous50342275
124686998646869987GGT10GENICheterozygous50454207
124687009846870099TC13GENIChomozygous50221196
124687021246870213CA20GENIChomozygous50611013
124687023546870236CG21GENIChomozygous50221198
124687036646870367CCG28GENIChomozygous50342277
124687049246870493TG14GENIChomozygous50221202
124687215246872153CT10GENIChomozygous50342279
124687240046872401TTG2GENIChomozygous50221230
124687304546873046GA18GENIChomozygous50342281
124687312846873129GA13GENIChomozygous50342283
124687331546873316AG16GENIChomozygous50221238
124687347746873478CT27GENIChomozygous50221239
124687370746873708AATGTGTGTG23GENIChomozygous50342285
124687514246875143AC29GENIChomozygous50221247
124687518246875183CT28GENICpossibly homozygous50342287
124687524446875245TTTGTGTG10GENICheterozygous50221249
124687542746875428CT24GENIChomozygous50342289
124687642746876432GCCCC-----2GENIChomozygous50221257
124687490746874917AAACCAAACC----------4GENIChomozygous50545794
124687524446875245TTTGTGTGTG10GENICheterozygous50545795
124687527246875273CCTG10GENICheterozygous50545796
124687527246875273CCTGTG10GENICheterozygous50545797
124687072346870735TGTGTGCGTGCA------------18GENIChomozygous50513420