chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115672801115672802AG52GENIChomozygous137189688
4115673394115673395C10GENICpossibly homozygous403818776
4115673394115673395CA10GENICheterozygous403818777
4115673397115673398C10GENICpossibly homozygous403818778
4115673397115673398CA10GENICheterozygous403818779
4115675216115675217AG46GENIChomozygous137189690
4115675797115675798TC38GENIChomozygous137189691
4115673400115673401C10GENICpossibly homozygous403991386
4115673400115673401CA10GENICheterozygous403991387
4115673406115673407C10GENICpossibly homozygous404067141
4115673406115673407CA10GENICheterozygous404067142
4115674154115674155CG38GENIChomozygous143148402
4115675407115675408TC45GENIChomozygous143148403
4115675812115675813AC36GENIChomozygous143148404
4115677629115677630TC47GENIChomozygous143148405
4115674730115674731C10GENICheterozygous403717001
4115674730115674731CT10GENIChomozygous403717002
4115693545115693546TC53GENIChomozygous137189705
4115674431115674431GTGTGTATGTTTGTGTGTACAT46GENIChomozygous143060199
4115678796115678797GA46GENIChomozygous143148406
4115680151115680152GT37GENIChomozygous143148407
4115680897115680898TC61GENIChomozygous137189697