chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1204836991204836992AG17GENIChomozygous75735701
1204837794204837795GT17GENIChomozygous76108074
1204837861204837862TC27GENIChomozygous75735703
1204838609204838610GA29GENIChomozygous76108075
1204838892204838893AG28GENIChomozygous74678285
1204839356204839357CA26GENIChomozygous75735704
1204839447204839448CA22GENIChomozygous76108076
1204842984204842985GA28GENIChomozygous74678289
1204843595204843596TC18GENIChomozygous74678291
1204845150204845151TC31GENIChomozygous74678293
1204845891204845892AG26GENIChomozygous74678295
1204846036204846037TG41GENIChomozygous74678297
1204846351204846352GA24GENICpossibly homozygous74678299
1204846745204846746GA29GENIChomozygous74678301
1204848500204848501TC32GENIChomozygous74678303
1204849200204849201GA40GENIChomozygous74678307