chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG11GENIChomozygous61226302
1274246689274246690TC12GENIChomozygous61226303
1274246937274246938GGTGGA8GENIChomozygous61226304
1274248204274248205TC4GENIChomozygous61226307
1274248238274248239GGAAAA4GENIChomozygous62217567
1274249892274249893AG4GENIChomozygous61226309
1274250311274250312CCT3GENIChomozygous61226311
1274251158274251159AG9GENIChomozygous61226312
1274251847274251848T-7GENIChomozygous61226313
1274252096274252099GGA---9GENIChomozygous61226314
1274252729274252730AG13GENICpossibly homozygous61226315
1274255130274255131TC7GENIChomozygous61226316
1274255731274255732TTCACACACA3GENICheterozygous61226318
1274256816274256817TC10GENIChomozygous61226320
1274256846274256847CT8GENIChomozygous61226321
1274256878274256879GA4GENIChomozygous61226322
1274256910274256911CCA2GENIChomozygous61226324
1274257373274257374TC6GENIChomozygous61226327