chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1255570722255570723TC18GENIChomozygous108618532
1255570864255570865GA32GENICpossibly homozygous120604746
1255580093255580094GA31GENIChomozygous108618544
1255585658255585659GA32GENIChomozygous120604748
1255592548255592549TA6GENIChomozygous109375666
1255595447255595448TG21GENIChomozygous108618578
1255595457255595458GA21GENIChomozygous108618580
1255598391255598392GC17GENIChomozygous108618584
1255599082255599083AG25GENIChomozygous108618588
1255599536255599537AC17GENICheterozygous120512658
1255601258255601259AG16GENIChomozygous120604750
1255601377255601378GC11GENICpossibly homozygous108618592
1255601894255601895CT9GENIChomozygous120604752
1255603476255603477AT26GENIChomozygous120604754
1255604572255604573CT17GENIChomozygous120604756
1255605102255605103GA18GENIChomozygous120880387
1255605914255605915TA15GENIChomozygous108618598
1255608418255608419AC36GENIChomozygous108618600
1255609684255609685GA17GENIChomozygous108618604
1255612996255612997GA21GENIChomozygous120604758
1255613419255613420AG17GENIChomozygous120604760
1255619565255619566TG19GENIChomozygous120604764
1255622985255622986GA25GENIChomozygous108618616
1255623745255623746CA28GENIChomozygous120604766
1255624806255624807CT39GENIChomozygous108618620
1255626609255626610TA23GENIChomozygous108618624
1255628992255628993GA17GENIChomozygous108618628
1255631902255631903TG19GENIChomozygous120604768
1255632078255632079CT19GENIChomozygous120880388
1255638129255638130CT17GENIChomozygous120604770
1255638860255638861AG21GENIChomozygous108618645
1255644168255644169GA35GENIChomozygous109375723
1255644491255644492TG40GENIChomozygous108618651
1255648124255648125CT30GENIChomozygous109375729
1255648644255648645GA7GENIChomozygous108618654
1255650440255650441TG16GENIChomozygous108618656
1255651556255651557CT22GENIChomozygous120604772
1255652047255652048AG19GENIChomozygous108618658
1255654644255654645CG20GENIChomozygous120604774