chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3121728767121728768CT25GENIChomozygous112145012
3121728961121728962TG31GENIChomozygous112296966
3121729350121729351TA21GENIChomozygous112145015
3121730138121730139CT16GENIChomozygous112145019
3121730200121730201AT28GENIChomozygous112296968
3121730387121730388TG16GENIChomozygous111690013
3121730623121730624AG21GENIChomozygous111690014
3121730827121730828CT20GENIChomozygous112145021
3121731860121731861TC15GENIChomozygous112145026
3121731874121731875AG19GENIChomozygous112145028
3121731936121731937AG11GENIChomozygous112145030
3121732326121732327TC28GENIChomozygous112145032
3121732341121732342TC24GENIChomozygous111690017
3121733098121733099CT10GENIChomozygous112296970
3121733526121733527TC28GENIChomozygous112145034
3121733591121733592CT27GENIChomozygous112296972
3121734372121734373GA36GENIChomozygous112145036
3121734501121734502GT22GENIChomozygous112296974
3121734729121734730CG25GENIChomozygous112145038
3121737236121737237CT20GENIChomozygous112145046
3121737283121737284GA25GENIChomozygous112145048
3121738503121738504TC31GENIChomozygous112145052