chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109038326990383270C14GENIChomozygous128844154
109038333990383340T16GENIChomozygous128844156
109038414890384148GCGCGGGTGGCT10GENICpossibly homozygous131469393
109038543890385439AG25GENIChomozygous116904573
109038556490385565TC20GENIChomozygous116676198
109038671690386717AC39GENIChomozygous116676200
109038715990387159G20GENIChomozygous131469394
109038774890387749GA16GENIChomozygous116904575
109038838190388382GA19GENIChomozygous117020550
109038880790388808GA21GENIChomozygous116904577
109039038390390384GA20GENIChomozygous116676204
109039059690390596AAGAAAGA16GENIChomozygous131469395
109039220590392206CT18GENIChomozygous116676208
109039217690392177GC18GENIChomozygous117068533