chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
470771987077199AG17GENIChomozygous113433974
470779327077933GA13GENIChomozygous113433976
470795447079545AG7GENIChomozygous113077047
470804527080453TG9GENIChomozygous113077050
470808437080844AG13GENIChomozygous113077051
470832287083229GA19GENIChomozygous113433982
470833507083351CT17GENIChomozygous113433984
470838027083803TC22GENIChomozygous113077058
470839917083992GA12GENIChomozygous113433986
470842767084277TC18GENIChomozygous113077059
470867887086789GT14GENIChomozygous113433990
470878217087822TC8GENIChomozygous113433992
470879747087975TC15GENIChomozygous113077062
470895677089568TC19GENIChomozygous113077064
470901057090106GA14GENIChomozygous113433994
470909067090907TC19GENIChomozygous113077066
470921867092187AG9GENIChomozygous113433998
470934407093441CT17GENIChomozygous113434000
470935847093585CT24GENIChomozygous113434002
470941097094110TA17GENIChomozygous113077068
470949267094927GA26GENICpossibly homozygous113434004
470956557095656CT10GENIChomozygous113434006
470961867096187GA13GENIChomozygous113077070
470967627096763AG13GENIChomozygous113434008
471004167100417TG17GENIChomozygous113077075
471006197100620GT8GENIChomozygous113434012
471013307101331GA18GENIChomozygous113434014
471025817102582CT12GENIChomozygous113434018
471044357104436GA7GENIChomozygous113434020
471062017106202GA11GENIChomozygous113434022