chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG59GENIChomozygous61226302
1274246689274246690TC30GENIChomozygous61226303
1274246937274246938GGTGGA29GENIChomozygous61226304
1274248204274248205TC7GENIChomozygous61226307
1274248239274248242AAA---1GENIChomozygous61334087
1274249132274249133TTA17GENICheterozygous61334088
1274249619274249620CT14GENIChomozygous61334089
1274250311274250312CCT1GENIChomozygous61226311
1274250567274250568TC25GENIChomozygous61334090
1274251158274251159AG14GENIChomozygous61226312
1274251192274251193GA14GENIChomozygous61334091
1274251846274251847AAT22GENIChomozygous61334092
1274252096274252099GGA---14GENIChomozygous61226314
1274252729274252730AG47GENIChomozygous61226315
1274255130274255131TC41GENIChomozygous61226316
1274255731274255732TTCA12GENICpossibly homozygous61334093
1274256816274256817TC46GENIChomozygous61226320
1274256846274256847CT32GENICpossibly homozygous61226321
1274256878274256879GA8GENICpossibly homozygous61226322