chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1670884277088428CT24GENIChomozygous111712293
1670892017089202CG22GENIChomozygous112102817
1670892457089246GC10GENIChomozygous111712295
1670924167092417CT13GENIChomozygous119190793
1670940647094065GA25GENIChomozygous111712303
1670944817094482TC10GENIChomozygous112102819
1670945627094563CG17GENIChomozygous119190794
1670946407094641TC18GENIChomozygous119190795
1670946777094678GT23GENIChomozygous119190796
1670947537094754TC21GENICpossibly homozygous119190797
1670948137094814GA18GENIChomozygous119190798
1670948207094821CT19GENIChomozygous119190799
1670948397094840CT13GENIChomozygous119190800
1670948407094841GA13GENIChomozygous119190801
1670948467094847AT14GENIChomozygous119190802
1670948637094864AG12GENIChomozygous119190803
1670948767094877AG11GENIChomozygous119190804
1670948827094883TC14GENIChomozygous119190805
1670949057094906TC16GENIChomozygous119207769
1670954847095485TC7GENICheterozygous112346216