chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122354503823545039AG22GENIChomozygous988906815
122354722423547225GA29GENIChomozygous988906816
122354824023548241TC28GENIChomozygous988906817
122354965523549656CT47GENIChomozygous988906818
122354971023549711AG26GENIChomozygous988906819
122354987023549871TC28GENIChomozygous988906820
122355010723550108TC36GENIChomozygous988906821
122355016623550167CT29GENIChomozygous988906822
122355130623551307CT15GENIChomozygous988906823
122355152523551526CT23GENIChomozygous988906824
122355233623552337TC32GENIChomozygous988906825
122355254423552545TC26GENIChomozygous988906826
122355261823552619AG39GENIChomozygous988906827
122355344023553441CT30GENIChomozygous988906828
122355391023553911GA26GENIChomozygous988906829
122355616623556167CT25GENIChomozygous988906830
122355674723556748TC32GENIChomozygous988906831
122355679023556791AC27GENIChomozygous988906832
122355805123558052AC42GENIChomozygous988906833
122356027523560276AG24GENIChomozygous988906834
122356327823563279GA28GENIChomozygous988906835
122356338623563387TC35GENIChomozygous988906836