chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410380024103801TG16GENIChomozygous980261812
142410385924103860TA20GENIChomozygous980261813
142410427124104272TC43GENIChomozygous980261814
142410436724104368TC24GENIChomozygous980261815
142410441624104417GC29GENIChomozygous980261816
142410456424104565GA13GENIChomozygous980261817
142410471824104719GA16GENIChomozygous980261818
142410474224104743TC14GENIChomozygous980261819
142410961424109615TC18GENIChomozygous980261820
142410964224109643CT16GENIChomozygous980261821
142410982324109824GT23GENIChomozygous980261822
142410989424109895GT18GENIChomozygous980261823
142410999024109991GC28GENIChomozygous980261824
142411653724116538TC16GENIChomozygous980261825
142411671024116711GA12GENIChomozygous980261826
142411704524117046AC27GENIChomozygous980261827
142411943824119439TA27GENIChomozygous980261828
142411988824119889GA13GENIChomozygous980261829
142412123724121238GA10GENIChomozygous980261830
142412148724121488GA31GENIChomozygous980261831
142412186924121870AT48GENIChomozygous980261832
142412329224123293GT29GENIChomozygous980261833
142412331324123314GC28GENIChomozygous980261834
142412389124123892GC26GENIChomozygous980261835
142412462824124629AG4GENIChomozygous980261836
142412524224125243TC19GENIChomozygous980261837