chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120749745120749746A23GENIChomozygous128512379
7120749763120749763C22GENIChomozygous128512380
7120749768120749768C21GENIChomozygous128512381
7120749837120749837G14GENIChomozygous128512382
7120749840120749844CACT15GENIChomozygous128512383
7120749868120749868A15GENIChomozygous128512384
7120749879120749880GT15GENIChomozygous115856998
7120749884120749884A15GENIChomozygous128512385
7120749910120749911G17GENIChomozygous128512386
7120749917120749918T17GENIChomozygous128512387
7120749924120749924A19GENIChomozygous128512388
7120749943120749944A21GENIChomozygous128512389
7120749946120749946C21GENIChomozygous128512390
7120749980120749981C20GENIChomozygous128512391
7120749985120749985T22GENIChomozygous128512392
7120749994120749995A22GENIChomozygous128512393
7120750000120750001GC22GENIChomozygous115857000
7120750010120750010C20GENIChomozygous128512394
7120750018120750018C23GENIChomozygous128512395
7120750019120750020AC24GENIChomozygous118259121
7120750034120750036AT27GENIChomozygous128512396
7120750057120750058A24GENIChomozygous128512397
7120750074120750074G23GENIChomozygous128512398
7120750081120750081T23GENIChomozygous128512399
7120750093120750094AG24GENIChomozygous116081954
7120750098120750099AC24GENIChomozygous115857002
7120750109120750109G23GENIChomozygous128512400
7120750094120750095GA24GENIChomozygous116262908