chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
470771987077199AG13GENIChomozygous113433974
470778397077839CTTTATATTTCTAC14GENIChomozygous130925436
470779327077933GA15GENIChomozygous113433976
470795447079545AG11GENIChomozygous113077047
470804527080453TG14GENIChomozygous113077050
470808437080844AG18GENIChomozygous113077051
470809907080991GA8GENIChomozygous113077053
470816447081645TA13GENIChomozygous113433978
470817677081768AG14GENIChomozygous113433980
470832287083229GA16GENIChomozygous113433982
470833507083351CT14GENIChomozygous113433984
470838027083803TC21GENIChomozygous113077058
470839917083992GA9GENIChomozygous113433986
470842767084277TC11GENIChomozygous113077059
470867887086789GT18GENIChomozygous113433990
470878217087822TC22GENIChomozygous113433992
470879747087975TC17GENIChomozygous113077062
470892287089238AGGACAGGAC15GENIChomozygous130925437
470895677089568TC17GENIChomozygous113077064
470901057090106GA16GENIChomozygous113433994
470909067090907TC15GENIChomozygous113077066
470914397091440CT17GENIChomozygous113433996
470921867092187AG25GENIChomozygous113433998
470930377093037AAC27GENIChomozygous130925438
470934407093441CT33GENIChomozygous113434000
470935847093585CT14GENIChomozygous113434002
470941097094110TA14GENIChomozygous113077068
470972117097211CCAGCCA14GENIChomozygous130925439
471006197100620GT28GENIChomozygous113434012
470949267094927GA14GENIChomozygous113434004
470956557095656CT19GENIChomozygous113434006
470961867096187GA25GENIChomozygous113077070
470967627096763AG22GENIChomozygous113434008
470986637098664CT21GENIChomozygous113434010
471004167100417TG21GENIChomozygous113077075
471013307101331GA26GENIChomozygous113434014
471019237101924CG19GENIChomozygous113434016
471025817102582CT26GENIChomozygous113434018
471044357104436GA37GENIChomozygous113434020
471062017106202GA36GENIChomozygous113434022