chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122431910524319106TG6GENIChomozygous115287676
122431910624319107TC6GENIChomozygous115287678
122432003124320032TA13GENIChomozygous115422192
122432032424320325CT19GENIChomozygous115470143
122432083024320831AG12GENIChomozygous115493071
122432108124321082CG11GENIChomozygous115287682
122432108224321083CA10GENIChomozygous115287684
122432204624322047AG4GENIChomozygous115287688
122432264724322648TC20GENIChomozygous115287692
122432377924323780TA6GENICheterozygous115470145
122432403624324037CA19GENIChomozygous115470147
122432538324325384AT19GENIChomozygous115287696
122432631024326311CT25GENIChomozygous115470149
122432666724326668TC15GENIChomozygous115287702
122432698224326983CT13GENIChomozygous115287704
122432700424327005CT15GENIChomozygous115446760
122432810024328101CG18GENIChomozygous115287706
122432892224328923TC7GENICheterozygous115287708
122432905524329056TA14GENIChomozygous115446762
122432911224329113AG17GENIChomozygous115287710
122432931524329316CA18GENIChomozygous115470151
122432960224329603AC25GENIChomozygous115287712
122433129324331294GT21GENIChomozygous115287714
122433213724332138TC18GENIChomozygous115287716
122433329524333296CT12GENIChomozygous115446766
122433586824335869CT6GENIChomozygous115287718
122433631324336314CA10GENIChomozygous115446768
122433686424336865TC9GENIChomozygous115287720
122433752224337523CA9GENIChomozygous115287722