chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743757125743758G-6GENICheterozygous767735767
7125746090125746091CT35GENIChomozygous667652910
7125747342125747343CT15GENIChomozygous667652911
7125747534125747535CT25GENIChomozygous667652912
7125747571125747572GA26GENIChomozygous667652913
7125748329125748330AG19GENIChomozygous667652914
7125748832125748833C-1GENIChomozygous767735768
7125748927125748928GA27GENIChomozygous667652915
7125749012125749013GA22GENIChomozygous667652916
7125749414125749415AG19GENIChomozygous667652917
7125751521125751522AAT7GENICheterozygous767735769
7125751521125751522AATT7GENICpossibly homozygous767735770
7125752000125752001TC38GENIChomozygous667652918
7125752756125752757GA24GENIChomozygous667652919
7125753821125753822CT25GENIChomozygous667652920
7125753897125753898CT21GENIChomozygous667652921
7125753949125753950GA23GENIChomozygous667652922
7125754274125754275AG17GENIChomozygous667652923
7125754320125754321CT25GENIChomozygous667652924
7125754367125754368CT31GENIChomozygous667652925
7125754379125754380GC32GENIChomozygous667652926
7125755157125755158GA18GENIChomozygous667652927
7125755666125755667CT34GENIChomozygous667652928
7125755703125755704CT36GENIChomozygous667652929
7125756500125756501TC18GENIChomozygous667652930
7125756849125756850AG21GENIChomozygous667652931
7125756965125756966GGAAAA3GENIChomozygous767735772
7125757153125757154TTA17GENICpossibly homozygous767735774