chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG17GENIChomozygous61226302
1274246689274246690TC36GENIChomozygous61226303
1274246937274246938GGTGGA22GENIChomozygous61226304
1274248204274248205TC3GENIChomozygous61226307
1274248238274248239GGAAAA2GENIChomozygous62217567
1274249684274249685GA9GENIChomozygous61226308
1274249892274249893AG10GENIChomozygous61226309
1274250311274250312CCT5GENIChomozygous61226311
1274251158274251159AG13GENIChomozygous61226312
1274251847274251848T-15GENICpossibly homozygous61226313
1274252096274252099GGA---19GENIChomozygous61226314
1274252729274252730AG26GENIChomozygous61226315
1274255130274255131TC16GENIChomozygous61226316
1274255731274255732TTCACACACA7GENIChomozygous61226318
1274256816274256817TC24GENIChomozygous61226320
1274256846274256847CT12GENIChomozygous61226321
1274256878274256879GA5GENIChomozygous61226322
1274256892274256893A-5GENICheterozygous61334094
1274256910274256911CCA3GENIChomozygous61226324
1274257373274257374TC23GENIChomozygous61226327