chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG21GENIChomozygous61226302
1274246689274246690TC26GENIChomozygous61226303
1274246937274246938GGTGGA15GENIChomozygous61226304
1274247316274247317AAT1GENIChomozygous61334083
1274247318274247319AAT1GENIChomozygous61334084
1274247335274247336AT1GENIChomozygous61334086
1274248204274248205TC18GENIChomozygous61226307
1274248239274248242AAA---7GENICpossibly homozygous61334087
1274249132274249133TTA10GENICpossibly homozygous61334088
1274249619274249620CT12GENIChomozygous61334089
1274250311274250312CCT12GENICpossibly homozygous61226311
1274250567274250568TC18GENIChomozygous61334090
1274251158274251159AG25GENIChomozygous61226312
1274251192274251193GA19GENICpossibly homozygous61334091
1274251846274251847AAT27GENICpossibly homozygous61334092
1274252096274252099GGA---24GENIChomozygous61226314
1274252729274252730AG29GENIChomozygous61226315
1274255130274255131TC17GENIChomozygous61226316
1274255731274255732TTCA12GENICpossibly homozygous61334093
1274256816274256817TC13GENIChomozygous61226320
1274256846274256847CT11GENIChomozygous61226321
1274256878274256879GA10GENIChomozygous61226322
1274256892274256893A-7GENIChomozygous61334094
1274256910274256911CCAAAAA4GENIChomozygous62112749
1274256950274256951TTAA8GENIChomozygous62242478