chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG22GENIChomozygous61226302
1274246689274246690TC30GENIChomozygous61226303
1274246937274246938GGTGGA20GENIChomozygous61226304
1274248204274248205TC5GENIChomozygous61226307
1274248238274248239GGAAAA2GENICheterozygous62217567
1274249684274249685GA3GENIChomozygous61226308
1274249892274249893AG9GENIChomozygous61226309
1274250311274250312CCT1GENIChomozygous61226311
1274251158274251159AG11GENIChomozygous61226312
1274251847274251848T-21GENIChomozygous61226313
1274252096274252099GGA---20GENIChomozygous61226314
1274252729274252730AG32GENIChomozygous61226315
1274255130274255131TC15GENIChomozygous61226316
1274255731274255732TTCACACACA8GENICpossibly homozygous61226318
1274256816274256817TC10GENIChomozygous61226320
1274256846274256847CT8GENIChomozygous61226321
1274256878274256879GA5GENIChomozygous61226322
1274256910274256911CCA1GENIChomozygous61226324
1274257373274257374TC17GENIChomozygous61226327