chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5150033958150033959TC16GENIChomozygous114054667
5150034287150034288AG11GENIChomozygous114054669
5150034347150034348AG18GENIChomozygous114054670
5150034367150034368AG14GENIChomozygous114054672
5150034561150034562GA15GENIChomozygous114054674
5150034749150034750CT24GENIChomozygous114054676
5150036681150036682AG13GENIChomozygous114054678
5150037426150037427AC20GENIChomozygous114054680
5150038106150038107TC14GENIChomozygous114054682
5150039488150039489AG11GENICheterozygous114054686
5150039681150039682AT3GENICheterozygous114054688
5150040107150040108AG22GENIChomozygous114054690
5150040588150040589AG23GENIChomozygous114054692
5150041121150041122GT17GENIChomozygous114054694
5150043963150043964GT25GENIChomozygous114054696
5150045785150045786AG26GENIChomozygous114054698
5150046685150046686CT24GENIChomozygous114054700
5150051896150051897GA12GENIChomozygous114054704