chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212232148212232149CA17GENIChomozygous940093578
1212232401212232402GT28GENIChomozygous940093579
1212232675212232676AG32GENIChomozygous940093580
1212234575212234576CT24GENIChomozygous940093581
1212234680212234681CT37GENIChomozygous940093582
1212234842212234843GA33GENIChomozygous940093583
1212235696212235697TC28GENIChomozygous940093584
1212235726212235727GA35GENIChomozygous940093585
1212236314212236315AG31GENIChomozygous940093586
1212237796212237797TA25GENIChomozygous940093587
1212238003212238004CT22GENIChomozygous940093588
1212238216212238217GA21GENIChomozygous940093589
1212240228212240229CT17GENIChomozygous940093590
1212240599212240600CT37GENIChomozygous940093591
1212245421212245422GC29GENIChomozygous940093592
1212246250212246251GA39GENIChomozygous940093593
1212246483212246484GA30GENIChomozygous940093594
1212246839212246840TC24GENIChomozygous940093595
1212246883212246884GT22GENIChomozygous940093596
1212246890212246891CT21GENIChomozygous940093597
1212246939212246940CG32GENIChomozygous940093598
1212247414212247415CT23GENIChomozygous940093599
1212248070212248071TC31GENIChomozygous940093600
1212248719212248720TC9GENIChomozygous940093601
1212249516212249517GA15GENIChomozygous940093602
1212249751212249752CT16GENIChomozygous940093603
1212254921212254922GC41GENIChomozygous940093604
1212255735212255736CA40GENIChomozygous940093605
1212256305212256306AG32GENIChomozygous940093606
1212259075212259076GA24GENIChomozygous940093607
1212260007212260008TC29GENIChomozygous940093608
1212267724212267725AG19GENIChomozygous940093609
1212268387212268388AG32GENIChomozygous940093610
1212269320212269321GA31GENIChomozygous940093611
1212272665212272666GT29GENIChomozygous940093612
1212274307212274308GT31GENIChomozygous940093613
1212275844212275845CA35GENIChomozygous940093614
1212276122212276123CT29GENIChomozygous940093615
1212276381212276382CT32GENIChomozygous940093616
1212278108212278109GA25GENIChomozygous940093617
1212278160212278161GA24GENIChomozygous940093618