chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG40GENIChomozygous61226302
1274246689274246690TC46GENIChomozygous61226303
1274246937274246938GGTGGA44GENIChomozygous61226304
1274248204274248205TC24GENIChomozygous61226307
1274248238274248239GGAAAA13GENICheterozygous62217567
1274249684274249685GA8GENIChomozygous61226308
1274249892274249893AG20GENIChomozygous61226309
1274250311274250312CCT14GENICpossibly homozygous61226311
1274251158274251159AG21GENIChomozygous61226312
1274251847274251848T-38GENIChomozygous61226313
1274252096274252099GGA---20GENIChomozygous61226314
1274252729274252730AG39GENIChomozygous61226315
1274255130274255131TC42GENIChomozygous61226316
1274255731274255732TTCACACACA11GENICheterozygous61226318
1274255731274255732TTCACACACACA11GENICheterozygous62242477
1274256816274256817TC44GENIChomozygous61226320
1274256846274256847CT32GENIChomozygous61226321
1274256878274256879GA21GENICpossibly homozygous61226322
1274256910274256911CCA4GENIChomozygous61226324
1274256950274256951TTAA5GENICheterozygous62242478
1274257373274257374TC47GENIChomozygous61226327