chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3121725513121725514GA4GENIChomozygous112296962
3121728207121728208GA10GENIChomozygous112145008
3121728767121728768CT8GENIChomozygous112145012
3121728961121728962TG11GENIChomozygous112296966
3121729350121729351TA11GENIChomozygous112145015
3121730138121730139CT14GENIChomozygous112145019
3121730200121730201AT11GENIChomozygous112296968
3121730387121730388TG11GENIChomozygous111690013
3121730623121730624AG8GENIChomozygous111690014
3121730827121730828CT8GENIChomozygous112145021
3121731860121731861TC11GENIChomozygous112145026
3121731874121731875AG12GENIChomozygous112145028
3121731936121731937AG7GENIChomozygous112145030
3121732326121732327TC10GENIChomozygous112145032
3121732341121732342TC8GENIChomozygous111690017
3121733098121733099CT5GENIChomozygous112296970
3121733526121733527TC9GENIChomozygous112145034
3121733591121733592CT12GENIChomozygous112296972
3121734372121734373GA5GENIChomozygous112145036
3121734501121734502GT13GENIChomozygous112296974
3121734729121734730CG11GENIChomozygous112145038
3121737236121737237CT12GENIChomozygous112145046
3121737283121737284GA11GENIChomozygous112145048
3121738503121738504TC17GENIChomozygous112145052