chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1274245290274245291CT56GENIChomozygous108654239
1274245513274245514GT56GENIChomozygous108654241
1274247017274247018TC60GENIChomozygous108654243
1274247432274247433GA57GENIChomozygous108654245
1274248132274248133GA57GENIChomozygous108654246
1274248379274248380CA18GENICheterozygous108654248
1274249342274249343TC54GENIChomozygous108654250
1274249538274249539AG39GENIChomozygous108654252
1274249982274249983GA43GENIChomozygous108654253
1274250089274250090CT45GENIChomozygous108654255
1274250098274250099GA44GENIChomozygous108654257
1274250546274250547GC18GENIChomozygous108654260
1274250610274250611TC36GENIChomozygous108654262
1274254807274254808AG61GENIChomozygous108654265
1274257057274257058TC55GENIChomozygous108654266
1274257513274257514GC72GENIChomozygous108654268
1274258420274258421AG29GENIChomozygous108654269
1274248375274248375A17GENICheterozygous130218563
1274251724274251724TATC50GENIChomozygous127512850
1274258585274258585AAAAAT31GENIChomozygous127512852