chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115672801115672802AG75GENIChomozygous137189688
4115673394115673395C8GENIChomozygous403818776
4115673394115673395CA8GENICheterozygous403818777
4115673397115673398C7GENICheterozygous403818778
4115674862115674863CT64GENIChomozygous137189689
4115675216115675217AG58GENIChomozygous137189690
4115675797115675798TC57GENIChomozygous137189691
4115676428115676429GT53GENIChomozygous137189692
4115677224115677225CA51GENIChomozygous137189693
4115678410115678411GA56GENIChomozygous137189694
4115679531115679532GA58GENICpossibly homozygous137189695
4115680176115680177AT45GENIChomozygous137189696
4115680897115680898TC58GENIChomozygous137189697
4115685097115685098TC34GENIChomozygous137189698
4115686860115686861CT61GENIChomozygous137189699
4115687628115687629CT52GENIChomozygous137189700
4115687680115687681AG55GENIChomozygous137189701
4115688584115688585TC67GENIChomozygous137189702
4115690454115690456AG35GENIChomozygous136910641
4115673397115673398CA7GENICheterozygous403818779
4115675003115675003T64GENIChomozygous136910639
4115684494115684498CCCA25GENIChomozygous136910640
4115690011115690012CT56GENIChomozygous137189703
4115690405115690406CT51GENIChomozygous137189704
4115673400115673401C7GENICheterozygous403991386
4115673400115673401CA7GENICheterozygous403991387
4115674730115674731C14GENICheterozygous403717001
4115674730115674731CT14GENIChomozygous403717002
4115693545115693546TC47GENIChomozygous137189705
4115693871115693872GA49GENIChomozygous137189706
4115694874115694875GA63GENIChomozygous137189707
4115694992115694993TC58GENIChomozygous137189708
4115695200115695201CT71GENIChomozygous137189709
4115697736115697737TC53GENICpossibly homozygous137189710
4115698947115698948AG69GENIChomozygous137189711
4115701517115701518CT66GENIChomozygous137189712
4115703230115703231CT58GENIChomozygous137189713