chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3165909771165909772GA22INTERGENIChomozygous72555549
3165914850165914851CT15INTERGENIChomozygous72555552
3165921855165921856GA3INTERGENIChomozygous72555590
3165924253165924254CT30INTERGENIChomozygous72555593
3165936754165936755GA15INTERGENIChomozygous72555604
3165938698165938699AG21INTERGENIChomozygous72286892
3165938717165938718TG18INTERGENIChomozygous72286893
3165939817165939818GC26INTERGENICpossibly homozygous72555610
3165941415165941416TC9INTERGENIChomozygous72555613
3165941690165941691GT14INTERGENIChomozygous72555616
3165957695165957696AC14INTERGENIChomozygous72555619
3165961814165961815TA18INTERGENIChomozygous72555622
3165965426165965427AG33INTERGENICheterozygous72286899
3165965446165965447TA42INTERGENICheterozygous72286900
3165965498165965499CT32INTERGENICheterozygous72555631
3165965587165965588TC49INTERGENICheterozygous72286901
3165965619165965620GA37INTERGENICheterozygous72286902
3165965635165965636CG49INTERGENICheterozygous72286903
3165965668165965669TG59INTERGENICheterozygous72286904
3165966544165966545TA44INTERGENICheterozygous72286923
3165967225165967226GT36INTERGENIChomozygous72286925
3165967262165967263CA12INTERGENIChomozygous72286926
3165968775165968776GA12INTERGENICheterozygous72555643
3165968474165968475AG17INTERGENICheterozygous73168672