chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
194901912149019122GA23GENIChomozygous109721727
194901995449019955GA35GENIChomozygous109721729
194902025649020257AT15GENIChomozygous109721730
194902027849020279AG15GENIChomozygous109721732
194902071749020718TG22GENIChomozygous109721734
194902156649021567GA24GENIChomozygous109721736
194902351149023512TC28GENIChomozygous109721738
194902367949023680GA23GENICpossibly homozygous109721740
194902427349024274GA23GENIChomozygous109721742
194902470449024705GA37GENIChomozygous109721746
194902482849024829GA22GENIChomozygous109721748
194902531149025312GA29GENIChomozygous109721752
194902535149025352GT29GENIChomozygous109721754
194902603749026038AC14GENIChomozygous109721756
194902608149026082AG24GENIChomozygous109721758
194902609349026094AG27GENIChomozygous109721760
194902693449026935GA18GENIChomozygous109721762
194902693649026937CG18GENIChomozygous109721764
194902710249027103GA19GENIChomozygous109721766
194902723749027238TC27GENIChomozygous109721768
194902752749027528GA23GENIChomozygous109721770
194902561549025616CT15GENIChomozygous109820740