chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245567274245568GA49GENIChomozygous109383306
1274247222274247223GC55GENIChomozygous109383308
1274247432274247433GA65GENIChomozygous108654245
1274248132274248133GA55GENIChomozygous108654246
1274248379274248380CA28GENICheterozygous108654248
1274248720274248721CT46GENIChomozygous109383310
1274249342274249343TC52GENIChomozygous108654250
1274249538274249539AG54GENIChomozygous108654252
1274250098274250099GA56GENIChomozygous108654257
1274250546274250547GC34GENIChomozygous108654260
1274250610274250611TC52GENIChomozygous108654262
1274251961274251962AT56GENIChomozygous109383312
1274253118274253119CT66GENIChomozygous109383314
1274254254274254255CA61GENIChomozygous109383315
1274254807274254808AG60GENIChomozygous108654265
1274256030274256031GA47GENIChomozygous109383317
1274257513274257514GC59GENIChomozygous108654268
1274258420274258421AG45GENIChomozygous108654269
1274258585274258585AAAAAT51GENIChomozygous127512852
1274248375274248375A25GENICheterozygous130218563
1274248847274248850TCC40GENIChomozygous130837282
1274253089274253089GCGTCTGTGT55GENIChomozygous127512851