chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135578917355789176TTC---1GENIChomozygous732107685
135578922755789228TTC6GENIChomozygous732107686
135578927055789271TTTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC5GENIChomozygous732107687
135578942255789423CG20GENIChomozygous608602497
135578961755789618GGTC4GENICheterozygous732107689
135578965455789656TC--4GENICheterozygous732107690
135578972455789725TTC2GENIChomozygous732107691
135578973155789732CCTCT3GENIChomozygous732107692
135579103355791034GA17GENIChomozygous605710778
135579172455791726CA--19GENIChomozygous732107693
135579200955792010GGCA13GENICheterozygous732107694
135579200955792010GGCACA13GENICheterozygous732107695
135579200955792010GGCACACA13GENICheterozygous732107696
135579237255792373TG21GENIChomozygous608602498
135579258555792586GC14GENIChomozygous608602499
135579303055793031AG21GENIChomozygous605710779
135579307355793074T-21GENIChomozygous732107697
135579400355794004GA17GENIChomozygous608602500
135579446155794462CT31GENIChomozygous605710780
135579512755795128AG28GENIChomozygous605710781
135579548355795484TC24GENIChomozygous605710782
135579568655795687GGC19GENIChomozygous732107698
135579620255796203CT30GENIChomozygous608602501
135579709655797097CT23GENICpossibly homozygous608602502
135579731455797315GA16GENIChomozygous608602503
135579807855798079AACCCC4GENIChomozygous732107700
135579838855798389AAGACTGACT8GENIChomozygous732107703
135579909955799100AC25GENIChomozygous605710783
135579987755799878AG33GENIChomozygous605710784
135580022155800222CT16GENIChomozygous608602504
135580029355800294GC23GENIChomozygous608602505
135580048755800488AT18GENIChomozygous608602506
135580062355800624CG13GENIChomozygous605710785
135580108355801086TGG---16GENIChomozygous732107705
135580158155801582TC24GENIChomozygous608602507
135580164955801650AG17GENIChomozygous605710786
135580172555801726AG29GENIChomozygous605710787