chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
93963696739636968CG16GENIChomozygous117325884
93971393639713937CT20GENIChomozygous117326082
93974555739745558TA21GENIChomozygous117326233
93979307939793080GT20GENIChomozygous117805467
93980733839807339AG29GENIChomozygous117326571
93981256839812569AC28GENIChomozygous117530471
93981258839812589GA34GENIChomozygous117326619
93981348139813482CG25GENIChomozygous117530493
93988773939887740GA27GENIChomozygous117706317
93991153839911539CA21GENIChomozygous117792976
93991154039911541AG22GENIChomozygous117495313
93991160039911601TA26GENIChomozygous117326879
93991160439911605GT25GENIChomozygous117326880
93991788639917887TG32GENIChomozygous117326895
93991791339917914TG27GENIChomozygous117326896
93994257939942580GC26GENIChomozygous117326943
93994280239942803GT30GENIChomozygous117531033
93997570039975701TC17GENIChomozygous117706319
93997570239975703AT17GENIChomozygous117327132
93997570439975705TG17GENIChomozygous117327133
93997592539975926AC17GENIChomozygous117531368
93997597639975977AC15GENIChomozygous117531370
93997597739975978CT15GENIChomozygous117531372
93999074239990743TA24GENIChomozygous117327166