chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159979749159979750GGT22GENIChomozygous55814946
5159991081159991094CGCCACCCCCCCA-------------10GENIChomozygous55814966
5159991083159991093CCACCCCCCC----------10GENIChomozygous55814967
5159991112159991113TG19GENIChomozygous55814969
5159991117159991118TG19GENIChomozygous55814970
5159991122159991123TG19GENIChomozygous55814971
5159991127159991128TG19GENIChomozygous55814972
5160005781160005782CCT10GENIChomozygous55815009
5160006118160006119C-11GENIChomozygous55815010
5160017781160017782AG11GENIChomozygous55815037
5160017796160017797AG12GENIChomozygous55815039
5160018434160018435TTAC15GENICheterozygous55815042
5160018446160018447TC15GENICheterozygous56071894
5160022609160022610T-1GENIChomozygous55815050
5160042358160042359TG15GENICheterozygous55815086
5160042547160042549GT--10GENICheterozygous55815087
5160047060160047062TG--15GENIChomozygous55815094
5160050742160050743TG26GENICheterozygous55815108
5160050764160050765GT29GENICheterozygous55815109
5160059541160059542CG26GENICheterozygous56071895