chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12919147229191473GA29GENIChomozygous109069055
12919195129191952CT54GENIChomozygous109069057
12919235329192354AC64GENIChomozygous109069059
12919249129192492AT54GENIChomozygous108704814
12919251929192520TC49GENIChomozygous109069061
12919256629192567CG42GENIChomozygous108704816
12919302129193022TC49GENIChomozygous109069063
12919314829193149CT39GENIChomozygous109069065
12919321529193216CT37GENIChomozygous109069067
12919325429193255TG33GENIChomozygous108704818
12919403829194039CT56GENIChomozygous108066326
12919415629194157CT46GENIChomozygous109069069
12919422829194229CA35GENIChomozygous109069071
12919440329194404AG48GENIChomozygous109069073
12919440629194407AG48GENIChomozygous109069075
12919463429194635CT41GENIChomozygous109069077
12919466229194663AG37GENIChomozygous109069079
12919485629194857AG29GENIChomozygous108704822
12919536229195363TC49GENIChomozygous109069081
12919606529196066GA12GENICpossibly homozygous109069083
12919609729196098GA11GENIChomozygous109069085
12919614329196144AG29GENIChomozygous109069087
12919801529198016GA43GENIChomozygous109069089
12919851629198517AG28GENIChomozygous109069091
12919870829198709CT57GENICpossibly homozygous109069093
12919942129199422TG33GENIChomozygous108704834
12920021229200213TC50GENIChomozygous108704836
12920022829200229CA49GENIChomozygous109069094
12920034529200346AG42GENIChomozygous108704838
12920036229200363TA40GENIChomozygous108704840
12920072729200728CT48GENIChomozygous109069096
12920085429200855GA49GENIChomozygous109069098