chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136110536136110537GC9GENIChomozygous595626345
4136110720136110721GA15GENIChomozygous595626346
4136110835136110836AC22GENICpossibly homozygous595626347
4136110909136110910AG9GENIChomozygous595626348
4136110954136110955CT2GENIChomozygous595626349
4136110960136110961CG8GENIChomozygous595626350
4136111031136111032TC15GENICpossibly homozygous595626351
4136111098136111099CT18GENIChomozygous595626352
4136111170136111171GA17GENICpossibly homozygous595626353
4136111227136111228TA16GENICpossibly homozygous595626354
4136111299136111300AC19GENICpossibly homozygous595626355
4136111384136111385CG16GENIChomozygous595626356
4136111468136111469AC22GENIChomozygous595626357
4136111652136111653AG18GENIChomozygous595626358
4136111961136111962CT22GENICpossibly homozygous595626359
4136112159136112160TTCACCTGA2GENICheterozygous726991067
4136112220136112221CG12GENIChomozygous595626360
4136112376136112377TTCC13GENICheterozygous726991068
4136112628136112629GA15GENIChomozygous595626361
4136112694136112695AG25GENICpossibly homozygous595626362
4136112778136112779AG20GENIChomozygous595626363
4136113093136113094GA18GENIChomozygous595626364
4136113250136113251AG10GENICheterozygous595626365
4136113414136113416GG--1GENIChomozygous726991069
4136113453136113454GGTA1GENIChomozygous726991070
4136113461136113462AATG3GENIChomozygous726991071
4136113541136113542AC2GENIChomozygous595626366
4136113579136113580AC6GENICheterozygous595626367
4136113625136113626CT7GENICheterozygous595626368
4136113750136113751TG6GENIChomozygous595626369
4136113770136113771CG10GENICpossibly homozygous595626370
4136113933136113934TG9GENIChomozygous595626371
4136113975136113976AC27GENIChomozygous595626372
4136114069136114070GA25GENICpossibly homozygous598096567
4136114208136114209GA25GENIChomozygous595626373
4136114614136114615GA23GENIChomozygous595626374