chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578922755789228TTC6GENIChomozygous734267509
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC4GENIChomozygous734267510
135578942255789423CG31GENICpossibly homozygous612016757
135578961755789618GGTC7GENICpossibly homozygous734267512
135578965455789656TC--6GENICheterozygous734267513
135578972455789725TTC1GENIChomozygous734267514
135578973155789732CCTCT2GENIChomozygous734267515
135579103355791034GA41GENIChomozygous609142735
135579172455791726CA--49GENIChomozygous734267516
135579200955792010GGCA10GENICheterozygous734267517
135579200955792010GGCACA10GENICheterozygous734267518
135579237255792373TG25GENIChomozygous612016758
135579258555792586GC35GENIChomozygous612016759
135579303055793031AG14GENIChomozygous609142736
135579307355793074T-8GENIChomozygous734267520
135579400355794004GA12GENIChomozygous612016760
135579404555794047AA--6GENICheterozygous734267521
135579446155794462CT21GENIChomozygous609142737
135579512755795128AG23GENIChomozygous609142738
135579548355795484TC31GENIChomozygous609142739
135579568655795687GGC27GENIChomozygous734267522
135579620255796203CT33GENIChomozygous612016761
135579709655797097CT19GENIChomozygous612016762
135579731455797315GA18GENIChomozygous612016763
135579807855798079AACCCC6GENIChomozygous734267524
135579838855798389AAGACTGACT16GENIChomozygous734267527
135579909955799100AC34GENIChomozygous609142740
135579987755799878AG24GENIChomozygous609142741
135580022155800222CT16GENIChomozygous612016764
135580029355800294GC20GENIChomozygous612016765
135580048755800488AT16GENIChomozygous612016766
135580062355800624CG29GENIChomozygous609142742
135580108355801086TGG---35GENIChomozygous734267529
135580158155801582TC27GENIChomozygous612016767
135580164955801650AG34GENIChomozygous609142743
135580172555801726AG40GENIChomozygous609142744