chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8103303487103303488CA21GENIChomozygous138400740
8103303787103303788CG20GENIChomozygous138400741
8103304109103304110AG17GENIChomozygous138400742
8103304227103304228AC18GENIChomozygous138400743
8103304436103304437CT17GENIChomozygous138400744
8103304485103304486CT14GENIChomozygous138400745
8103305007103305008TC27GENIChomozygous138400746
8103305305103305306CT23GENIChomozygous138400747
8103306650103306651GA20GENIChomozygous138400748
8103308794103308795GT17GENIChomozygous138400749
8103311927103311928GA22GENIChomozygous138400750
8103313605103313606AG21GENIChomozygous138400751
8103313983103313984AG24GENIChomozygous138400752
8103314153103314154CT32GENIChomozygous138400753
8103314197103314198CG25GENIChomozygous138400754
8103314200103314201AG26GENIChomozygous138400755
8103314727103314727C21GENIChomozygous138261308
8103308787103308787G14GENIChomozygous138261306
8103312945103312945C13GENIChomozygous138261307
8103313349103313350GA22GENICpossibly homozygous144396680
8103315221103315222GC19GENIChomozygous138400756
8103315703103315704TC17GENIChomozygous138400757