chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245548274245549AG50GENIChomozygous61226302
1274246689274246690TC31GENIChomozygous61226303
1274246937274246938GGTGGA24GENIChomozygous61226304
1274247294274247295TC13GENICheterozygous61226305
1274247320274247321AAAT1GENIChomozygous61226306
1274248204274248205TC15GENIChomozygous61226307
1274249684274249685GA3GENIChomozygous61226308
1274249892274249893AG11GENIChomozygous61226309
1274250249274250250GGAA3GENIChomozygous61226310
1274250311274250312CCT7GENIChomozygous61226311
1274251158274251159AG16GENIChomozygous61226312
1274251847274251848T-17GENIChomozygous61226313
1274252096274252099GGA---7GENIChomozygous61226314
1274252729274252730AG43GENIChomozygous61226315
1274255130274255131TC13GENIChomozygous61226316
1274255731274255732TTCACACA13GENICheterozygous61226317
1274255731274255732TTCACACACA13GENICheterozygous61226318
1274256816274256817TC18GENIChomozygous61226320
1274256846274256847CT16GENICheterozygous61226321
1274256878274256879GA13GENICheterozygous61226322
1274256892274256893A-4GENICheterozygous61334094
1274256910274256911CCA3GENICheterozygous61226324
1274257373274257374TC30GENIChomozygous61226327