chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6123206578123206579GA8GENIChomozygous126364873
6123257614123257615CT7GENIChomozygous126364886
6123257633123257634GT4GENIChomozygous126364888
6123257648123257649AT5GENIChomozygous126364890
6123257713123257714CA10GENIChomozygous126364892
6123257933123257934GA5GENIChomozygous126364902
6123258012123258013GT17GENIChomozygous126364904
6123285772123285773TC4GENIChomozygous126372613
6123311346123311347CA12GENIChomozygous126364906
6123311356123311357CA9GENIChomozygous126364908
6123311388123311389GA13GENIChomozygous126364910
6123338312123338313TA7GENIChomozygous114975229
6123338313123338314TA7GENICheterozygous114975230
6123338315123338316TA6GENIChomozygous126364916
6123338403123338404CT10GENIChomozygous126364918
6123341126123341127CG14GENIChomozygous126364920
6123348335123348336GC3GENICheterozygous126372614
6123354747123354748CG7GENIChomozygous126364936
6123354770123354771CG8GENIChomozygous126364938
6123376747123376748CT18GENIChomozygous126372615
6123403286123403287GA3GENICheterozygous126372616
6123418119123418120AG4GENICheterozygous126372617
6123475440123475441CG3GENICheterozygous126372618
6123518492123518493CT7GENICheterozygous115288257
6123518520123518521TC13GENICheterozygous114975662
6123559969123559970CT9GENICheterozygous114975717
6123560038123560039AT3GENICheterozygous115288289
6123560070123560071AT3GENICheterozygous126372619