chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106434976164349762CCT4GENICheterozygous51476380
106434976164349762CCTTT4GENICheterozygous52381530
106434976264349763T-4GENICheterozygous51987614
106435115064351151GGGA14GENIChomozygous51904686
106435121564351216AAGGGGCTGGGGATTTAGCTCAGT7GENIChomozygous52381532
106435130064351309AAAAACAAG---------2GENICheterozygous52381534
106435130564351309CAAG----2GENICheterozygous52381536
106435200464352005GA24GENIChomozygous51904688
106435206764352068CCCTT23GENIChomozygous51476382
106435344364353444GA27GENIChomozygous51904690
106435378164353782GA20GENIChomozygous51904692
106435544964355450GGAAAAAAAGAACCA3GENIChomozygous52381538
106435607164356072GA35GENIChomozygous51904694
106435770364357704AAAAAC11GENICheterozygous51674169
106435934364359344TC14GENIChomozygous51904696
106435978264359783TTC8GENIChomozygous52381540
106436043364360434A-7GENICheterozygous51674177
106436068264360683AG18GENIChomozygous51904700
106436144664361447GA23GENIChomozygous51904702
106436320664363207GGAA15GENICheterozygous52381542
106436320664363207GGA15GENICheterozygous52320117
106436674464366745CA26GENIChomozygous51904704
106436725564367256GA5GENIChomozygous51904706
106436750964367510GA20GENIChomozygous51674195
106436986064369861AAATAATG20GENIChomozygous51904710
106437016964370170GA20GENIChomozygous51904715
106437023464370235AG21GENIChomozygous51674201
106437046764370468AG22GENIChomozygous51674203
106437048064370481AG19GENIChomozygous51674205
106437108764371088GGCGCGCACACACA4GENICheterozygous52381544
106437108764371088GGCGCGCACACACACA4GENICheterozygous52381546