chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG31GENIChomozygous61226302
1274246689274246690TC31GENIChomozygous61226303
1274246937274246938GGTGGA17GENIChomozygous61226304
1274248204274248205TC13GENIChomozygous61226307
1274248238274248239GGAAAA7GENICpossibly homozygous62217567
1274249684274249685GA10GENICpossibly homozygous61226308
1274249892274249893AG9GENIChomozygous61226309
1274250311274250312CCT10GENIChomozygous61226311
1274251158274251159AG18GENIChomozygous61226312
1274251847274251848T-21GENIChomozygous61226313
1274252096274252099GGA---23GENIChomozygous61226314
1274252729274252730AG23GENIChomozygous61226315
1274255130274255131TC30GENIChomozygous61226316
1274255731274255732TTCACACACA6GENICheterozygous61226318
1274256816274256817TC19GENICpossibly homozygous61226320
1274256846274256847CT18GENIChomozygous61226321
1274256878274256879GA11GENIChomozygous61226322
1274256910274256911CCA5GENICheterozygous61226324
1274256950274256951TTAA2GENICheterozygous62242478
1274257373274257374TC22GENIChomozygous61226327