chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124128156941281570CA14GENIChomozygous115477961
124128207541282076AG26GENIChomozygous115329828
124128210241282103CT26GENIChomozygous115329830
124128216141282162AT32GENIChomozygous115329832
124128216241282163AT32GENIChomozygous115329834
124128217841282179AT31GENIChomozygous115329836
124128222641282227TG37GENIChomozygous115329838
124128225941282260CT34GENIChomozygous115329840
124128227741282278GA30GENIChomozygous115329842
124128227841282279CG30GENIChomozygous115329844
124128401941284020GT18GENIChomozygous115477967
124128402741284028CA19GENIChomozygous115477969
124128403441284035AC23GENIChomozygous115477971
124128403641284037TC23GENIChomozygous115477973
124128423441284235CA19GENIChomozygous115385012
124128424141284242TC19GENIChomozygous115385014
124128432141284322AG22GENIChomozygous115329848
124128437541284376GA19GENIChomozygous115329850
124128442141284422TC16GENIChomozygous115329852
124128470441284705AG14GENIChomozygous115329854
124128472741284728AG17GENIChomozygous115329856
124128472941284730TC17GENIChomozygous115329858
124128475141284752GA24GENIChomozygous115329860
124128495541284956AC22GENIChomozygous115329862
124128887841288879CG15GENIChomozygous115385030
124128899141288992GT19GENIChomozygous115385032
124128901741289018CT14GENIChomozygous115385034
124128904241289043TC8GENIChomozygous115385036
124128906941289070CA7GENICheterozygous115494910
124128908741289088GA5GENIChomozygous115385038
124128929341289294AG8GENIChomozygous115385040
124128966541289666AG12GENIChomozygous115385052
124128992041289921GA24GENIChomozygous115385056
124128398741283988GC15GENIChomozygous115610322