chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115672801115672802AG19GENIChomozygous137189688
4115673394115673395C8GENICheterozygous403818776
4115673394115673395CA8GENIChomozygous403818777
4115673397115673398C8GENICheterozygous403818778
4115673397115673398CA8GENIChomozygous403818779
4115675216115675217AG27GENIChomozygous137189690
4115675797115675798TC15GENIChomozygous137189691
4115674154115674155CG24GENIChomozygous143148402
4115675407115675408TC15GENIChomozygous143148403
4115675812115675813AC18GENIChomozygous143148404
4115677629115677630TC21GENICpossibly homozygous143148405
4115678796115678797GA16GENIChomozygous143148406
4115674730115674731C7GENICheterozygous403717001
4115674730115674731CT7GENICpossibly homozygous403717002
4115680151115680152GT19GENIChomozygous143148407
4115680897115680898TC26GENIChomozygous137189697
4115674431115674431GTGTGTATGTTTGTGTGTACAT18GENIChomozygous143060199
4115693545115693546TC14GENIChomozygous137189705