chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121960002019600021TC22GENIChomozygous115279489
121960051919600520AC9GENIChomozygous118248756
121960101819601019AC8GENIChomozygous118248757
121960104119601042GC11GENIChomozygous118248758
121960107519601076CA10GENIChomozygous118248759
121960118019601181CT16GENIChomozygous118248760
121960136919601370TG25GENIChomozygous115366036
121960161619601617AG32GENIChomozygous115279495
121960239019602391GA7GENIChomozygous115279497
121960573019605731AG9GENIChomozygous115366040
121960646719606468TC15GENIChomozygous115279499
121960803719608038GA6GENIChomozygous115279501
121960893619608937CA8GENIChomozygous115366042
121960898519608986CA6GENIChomozygous115279503
121960899419608995AG6GENIChomozygous115279505
121960900019609001GT7GENIChomozygous115279507
121960902519609026GT4GENIChomozygous115279509
121960949119609492CT8GENIChomozygous115366044
121961001019610011GA9GENIChomozygous115279511
121961271719612718GA8GENIChomozygous115445572
121961654119616542TC21GENIChomozygous115279515
121961877819618779GA20GENIChomozygous115279517
121961948319619484TC31GENIChomozygous115279519
121962032219620323CT29GENIChomozygous118248761
121962532519625326CT26GENIChomozygous118248762
121962624019626241TC38GENIChomozygous115279521
121962660719626608CT17GENIChomozygous115279523
121962661319626614TC19GENICpossibly homozygous115279525
121962758819627589GA21GENIChomozygous115279527
121962788119627882TG21GENIChomozygous115279529
121962918519629186AG16GENIChomozygous115279531
121961324919613250GA5GENIChomozygous115581170