chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
470771987077199AG28GENIChomozygous113433974
470778397077839CTTTATATTTCTAC37GENIChomozygous130925436
470779327077933GA51GENIChomozygous113433976
470795447079545AG20GENIChomozygous113077047
470804527080453TG44GENIChomozygous113077050
470808437080844AG39GENIChomozygous113077051
470809907080991GA17GENIChomozygous113077053
470816447081645TA50GENIChomozygous113433978
470817677081768AG21GENIChomozygous113433980
470832287083229GA55GENIChomozygous113433982
470833507083351CT39GENIChomozygous113433984
470838027083803TC42GENIChomozygous113077058
470839917083992GA47GENIChomozygous113433986
470842767084277TC41GENIChomozygous113077059
470867887086789GT36GENICpossibly homozygous113433990
470878217087822TC50GENIChomozygous113433992
470879747087975TC56GENIChomozygous113077062
470892287089238AGGACAGGAC32GENIChomozygous130925437
470895677089568TC51GENIChomozygous113077064
470901057090106GA52GENIChomozygous113433994
470909067090907TC35GENIChomozygous113077066
470914397091440CT18GENIChomozygous113433996
470921867092187AG49GENIChomozygous113433998
470930377093037AAC41GENIChomozygous130925438
470934407093441CT40GENIChomozygous113434000
470935847093585CT47GENIChomozygous113434002
470941097094110TA34GENIChomozygous113077068
470949267094927GA32GENICheterozygous113434004
470949287094929GA32GENICheterozygous131365969
470956557095656CT39GENICpossibly homozygous113434006
470961867096187GA61GENIChomozygous113077070
470967627096763AG45GENIChomozygous113434008
470972117097211CCAGCCA36GENIChomozygous130925439
470986637098664CT37GENIChomozygous113434010
471004167100417TG44GENIChomozygous113077075
471006197100620GT42GENICpossibly homozygous113434012
471013307101331GA35GENIChomozygous113434014
471019237101924CG42GENIChomozygous113434016
471025817102582CT32GENIChomozygous113434018
471044357104436GA40GENIChomozygous113434020
471062017106202GA40GENIChomozygous113434022