chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91966113719661138CT16GENIChomozygous52341948
91966399219663993CA10GENICpossibly homozygous51784792
91966629319666294CG15GENICpossibly homozygous52341950
91966674419666745T-2GENICheterozygous52466100
91967229519672296T-2GENICheterozygous53020042
91967244419672445GC17GENICpossibly homozygous51784808
91967287319672874TG7GENICheterozygous52341951
91967588619675887GA4GENICheterozygous51784811
91967817919678180CT8GENIChomozygous52341953
91967904419679045GGT2GENICheterozygous51784813
91968093819680939GA6GENICheterozygous52341955
91968970319689704TC8GENICheterozygous51784839
91969247619692480ATTC----3GENIChomozygous51784844
91969341519693416AG14GENICpossibly homozygous52341958
91969550219695503TTA1GENIChomozygous51784850
91969551319695514GT4GENIChomozygous51784851
91969551519695516GT5GENIChomozygous51784852
91969633819696339T-8GENICheterozygous51784854
91969875119698752TC16GENICpossibly homozygous51784862
91969930719699311TCTC----1GENIChomozygous53020054
91970230619702307TC9GENICpossibly homozygous51784865
91970658119706582CA6GENIChomozygous52845553
91970658219706583AT6GENIChomozygous52901745
91970781719707818TC15GENIChomozygous51784873
91970816319708167TTTG----2GENIChomozygous51784874
91971168719711688CA13GENICpossibly homozygous52341962
91971327919713280AATG8GENIChomozygous51784887
91971378019713781AG9GENICheterozygous52341963
91971584719715848AG2GENIChomozygous51784890
91971765019717651TC2GENIChomozygous52341966
91971811719718167CGCACACACACACACACACACACACACACACACACACACACACACACACA--------------------------------------------------2GENICheterozygous53020068
91971930319719304CG10GENICheterozygous51784894