chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187743181377431814AC48GENIChomozygous110410683
187743188777431888TC72GENIChomozygous110410685
187743342277433423AC36GENICpossibly homozygous110410687
187743517577435176TC35GENIChomozygous110410689
187743770377437704TC14GENIChomozygous110410693
187743897777438978TC12GENIChomozygous110410695
187743903877439039TC12GENIChomozygous110500949
187743961077439611GT14GENIChomozygous110870434
187743984377439844GA4GENIChomozygous110870436
187744011777440118TC21GENIChomozygous110601439
187744105977441060AG33GENICpossibly homozygous110410701
187744190677441907CT7GENIChomozygous110410703
187744198777441988GC37GENIChomozygous110410705
187744270477442705GA36GENIChomozygous110410709
187744305077443051AT32GENIChomozygous110870438
187744306877443069AG30GENIChomozygous110410711
187744506077445061GA23GENIChomozygous110410713
187744559277445593CA23GENIChomozygous110410714
187744596877445969TC31GENIChomozygous110410718
187744690977446910AG33GENIChomozygous110410720
187744753977447540AG31GENIChomozygous110410722
187744762377447624TC38GENIChomozygous110410724
187744862277448623CT26GENIChomozygous110500959
187744881277448813TC39GENIChomozygous110410726
187744890777448908GT39GENIChomozygous110410728
187744999377449994CT44GENIChomozygous110500961