chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91966113719661138CT26GENICpossibly homozygous631681803
91966399219663993CA7GENICpossibly homozygous631681804
91966514919665155TTTTTT------1GENIChomozygous745740115
91966629319666294CG23GENICheterozygous631681805
91966674319666744CCT2GENICheterozygous745740118
91967244419672445GC21GENIChomozygous631681806
91967287319672874TG2GENIChomozygous631681807
91967588619675887GA4GENIChomozygous631681808
91967817919678180CT14GENICpossibly homozygous631681809
91968951319689514TC1GENIChomozygous631681810
91968970319689704TC12GENICheterozygous631681811
91968970719689708A-9GENICheterozygous745740119
91969247619692480ATTC----2GENIChomozygous745740120
91969341519693416AG24GENICheterozygous631681812
91969550219695503TTA1GENIChomozygous745740125
91969551319695514GT3GENIChomozygous631681813
91969551519695516GT5GENIChomozygous631681814
91969800419698008CTCT----6GENICheterozygous745740126
91969875119698752TC23GENICpossibly homozygous631681815
91970230619702307TC23GENICpossibly homozygous631681816
91970658119706582CA6GENICheterozygous631681817
91970658219706583AT6GENICheterozygous631681818
91970708319707084GGTTTTTTTT4GENIChomozygous745740128
91970781719707818TC18GENICpossibly homozygous631681819
91970816319708167TTTG----5GENIChomozygous745740129
91971168719711688CA13GENIChomozygous631681820
91971327919713280AATG18GENIChomozygous745740130
91971378019713781AG25GENICpossibly homozygous631681821
91971584719715848AG4GENIChomozygous631681822
91971765019717651TC5GENICheterozygous631681823
91971930319719304CG20GENICpossibly homozygous631681824