chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG21GENIChomozygous61226302
1274246689274246690TC20GENIChomozygous61226303
1274246937274246938GGTGGA18GENIChomozygous61226304
1274247294274247295TC12GENIChomozygous61226305
1274247320274247321AAAT8GENIChomozygous61226306
1274249684274249685GA12GENIChomozygous61226308
1274249892274249893AG14GENIChomozygous61226309
1274251158274251159AG15GENIChomozygous61226312
1274251847274251848T-20GENICpossibly homozygous61226313
1274252096274252099GGA---11GENIChomozygous61226314
1274252729274252730AG15GENIChomozygous61226315
1274255130274255131TC17GENIChomozygous61226316
1274257373274257374TC13GENIChomozygous61226327