chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176171582176171583AG35GENIChomozygous112218626
3176175114176175115TC39GENIChomozygous112218627
3176176944176176945TC71GENIChomozygous112218628
3176176995176176996AG71GENIChomozygous112218629
3176177011176177012AG69GENIChomozygous112218630
3176178800176178801TG30GENIChomozygous112218631
3176186233176186234TC47GENIChomozygous112218632
3176189640176189641TC49GENIChomozygous112218633
3176189728176189729AG28GENIChomozygous112218634
3176190306176190307CT22GENIChomozygous112218635
3176192429176192430AT27GENIChomozygous112218637
3176192627176192628AG41GENIChomozygous112218638
3176194362176194363AG44GENIChomozygous112218639
3176196768176196769CA39GENICpossibly homozygous112218640
3176198083176198084GT14GENIChomozygous112218641
3176198620176198621CT28GENIChomozygous112218642
3176199805176199806AG19GENIChomozygous112218643
3176200257176200258TC49GENIChomozygous112218644
3176202217176202218AG47GENIChomozygous112218645
3176209611176209612TG38GENIChomozygous112218648
3176211639176211640GA37GENIChomozygous112218649
3176212360176212361CG8GENIChomozygous112319237
3176216246176216247AT42GENIChomozygous112218650
3176212209176212210GA26GENIChomozygous112047833