chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12919147229191473GA39GENIChomozygous109069055
12919195129191952CT34GENIChomozygous109069057
12919235329192354AC25GENIChomozygous109069059
12919249129192492AT22GENIChomozygous108704814
12919251929192520TC20GENIChomozygous109069061
12919256629192567CG18GENIChomozygous108704816
12919256829192569GA18GENIChomozygous120478744
12919302129193022TC17GENIChomozygous109069063
12919314829193149CT20GENIChomozygous109069065
12919321529193216CT14GENIChomozygous109069067
12919325429193255TG11GENIChomozygous108704818
12919403829194039CT14GENIChomozygous108066326
12919409829194099TA18GENIChomozygous109261432
12919415629194157CT19GENIChomozygous109069069
12919422829194229CA18GENIChomozygous109069071
12919440329194404AG38GENIChomozygous109069073
12919440629194407AG36GENIChomozygous109069075
12919445229194453CG26GENIChomozygous120478745
12919463429194635CT23GENIChomozygous109069077
12919466229194663AG31GENIChomozygous109069079
12919485629194857AG12GENIChomozygous108704822
12919536229195363TC35GENIChomozygous109069081
12919606529196066GA20GENICpossibly homozygous109069083
12919609729196098GA20GENICpossibly homozygous109069085
12919614329196144AG24GENICpossibly homozygous109069087
12919801529198016GA24GENIChomozygous109069089
12919851629198517AG22GENIChomozygous109069091
12919870829198709CT22GENIChomozygous109069093
12919942129199422TG34GENIChomozygous108704834
12920021229200213TC22GENIChomozygous108704836
12920022829200229CA20GENIChomozygous109069094
12920034529200346AG24GENIChomozygous108704838
12920036229200363TA24GENIChomozygous108704840
12920072729200728CT12GENIChomozygous109069096
12920085429200855GA8GENIChomozygous109069098