chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143649841143649842GA18GENICpossibly homozygous55759837
5143650275143650276CT27GENIChomozygous55759838
5143650874143650875T-17GENIChomozygous56125364
5143652921143652922CCT14GENIChomozygous55759839
5143653053143653054TA7GENIChomozygous55759840
5143653705143653706T-3GENICheterozygous56458424
5143653825143653828TTT---7GENIChomozygous56125365
5143653991143653992AG10GENIChomozygous55759845
5143654022143654023CT7GENIChomozygous55759846
5143654077143654078TA5GENIChomozygous55759847
5143654078143654079TA5GENIChomozygous55759848
5143654180143654181CG20GENIChomozygous55759852
5143654080143654081TA6GENIChomozygous55759849
5143654087143654088TTA4GENICheterozygous55759850
5143654168143654169AG17GENIChomozygous55759851
5143654658143654659AG21GENIChomozygous55759854
5143656319143656320TC35GENIChomozygous55759855
5143657627143657628AAC4GENIChomozygous55759856
5143657632143657634GC--4GENIChomozygous55759857
5143657643143657644TTC4GENIChomozygous55759858
5143657653143657654A-4GENIChomozygous55759859
5143657656143657658CT--4GENIChomozygous55759860
5143657836143657837G-14GENIChomozygous55759861
5143663154143663155TTTGTG4GENICheterozygous55759868
5143663745143663746CCAA4GENICheterozygous55759869
5143663745143663746CCAAA4GENICheterozygous56494407
5143663904143663905AG24GENIChomozygous55759870
5143664036143664037A-16GENIChomozygous55759871
5143664037143664038AT16GENIChomozygous56355271
5143664536143664537AG14GENIChomozygous55759873