chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103799743103799744GC12GENIChomozygous117030764
10103800561103800562GA17GENIChomozygous116833943
10103803186103803187CT24GENIChomozygous116833947
10103803406103803407CT18GENIChomozygous116833949
10103804339103804340AG21GENIChomozygous116833951
10103804529103804530CT20GENIChomozygous116833953
10103804572103804573TC7GENIChomozygous116833955
10103805227103805228AG22GENIChomozygous116960984
10103805566103805567CT13GENIChomozygous116833957
10103806409103806410GA10GENIChomozygous116833959
10103806765103806766AG8GENIChomozygous116833961
10103806769103806770AC6GENIChomozygous116833963
10103810093103810094GA18GENIChomozygous116833971
10103810926103810927TC22GENICheterozygous116833973
10103811026103811027CT29GENIChomozygous116833975
10103811529103811530AG14GENIChomozygous116833977
10103812268103812269CT31GENIChomozygous116833979
10103812810103812811CG23GENICpossibly homozygous116833981
10103814013103814014GA12GENIChomozygous116833983
10103814670103814671GA20GENIChomozygous116833985
10103812846103812847CA12GENICheterozygous126489675