chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG19GENIChomozygous61226302
1274246689274246690TC17GENIChomozygous61226303
1274246937274246938GGTGGA4GENICheterozygous61226304
1274248204274248205TC2GENICheterozygous61226307
1274249684274249685GA14GENICpossibly homozygous61226308
1274249892274249893AG5GENIChomozygous61226309
1274251158274251159AG15GENICpossibly homozygous61226312
1274251847274251848T-5GENICheterozygous61226313
1274252096274252099GGA---5GENICheterozygous61226314
1274252729274252730AG28GENICpossibly homozygous61226315
1274255130274255131TC22GENIChomozygous61226316
1274256816274256817TC12GENIChomozygous61226320
1274256846274256847CT2GENIChomozygous61226321
1274257373274257374TC9GENIChomozygous61226327