chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5153515677153515678AG22GENIChomozygous137654968
5153516144153516145AC31GENIChomozygous137654972
5153516164153516165AC28GENIChomozygous137654973
5153516614153516615GT12GENIChomozygous141766913
5153517041153517042CT5GENIChomozygous137654977
5153517910153517911TC25GENIChomozygous137654979
5153518027153518028GA11GENIChomozygous141766914
5153518797153518798CT11GENIChomozygous154258504
5153519657153519658CG20GENIChomozygous137654981
5153521968153521969CT20GENIChomozygous141766915
5153522163153522164AG14GENIChomozygous137654986
5153518797153518798C11GENICheterozygous403601375
5153517478153517479AT12GENICheterozygous403163436
5153517478153517479A12GENIChomozygous403163437
5153521358153521359T9GENIChomozygous137350050
5153517475153517479AATA12GENIChomozygous141691202
5153517510153517518AAAACAAA16GENIChomozygous141691203
5153517961153517961T14GENICpossibly homozygous141691204