chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176171582176171583AG45GENICpossibly homozygous112218626
3176172704176172705AT26GENIChomozygous111841358
3176175114176175115TC47GENIChomozygous112218627
3176176944176176945TC34GENIChomozygous112218628
3176176995176176996AG30GENIChomozygous112218629
3176177011176177012AG30GENIChomozygous112218630
3176178800176178801TG41GENIChomozygous112218631
3176186233176186234TC25GENIChomozygous112218632
3176189640176189641TC27GENIChomozygous112218633
3176189728176189729AG40GENIChomozygous112218634
3176190306176190307CT47GENICpossibly homozygous112218635
3176191367176191368AG21GENIChomozygous112218636
3176192429176192430AT48GENICpossibly homozygous112218637
3176192627176192628AG52GENIChomozygous112218638
3176194362176194363AG28GENIChomozygous112218639
3176196768176196769CA33GENIChomozygous112218640
3176198083176198084GT47GENIChomozygous112218641
3176198620176198621CT39GENIChomozygous112218642
3176199805176199806AG27GENIChomozygous112218643
3176200257176200258TC31GENIChomozygous112218644
3176202217176202218AG31GENIChomozygous112218645
3176202602176202603TC19GENIChomozygous111841360
3176202604176202605TC18GENIChomozygous111841362
3176202607176202608TC18GENIChomozygous111841364
3176207746176207747TA54GENICheterozygous112218646
3176208412176208413GC19GENIChomozygous112218647
3176208820176208821AC30GENIChomozygous111841366
3176209611176209612TG28GENIChomozygous112218648
3176211639176211640GA47GENICpossibly homozygous112218649
3176212209176212210GA26GENIChomozygous112047833
3176216246176216247AT38GENICpossibly homozygous112218650
3176212360176212361CG41GENIChomozygous112319237
3176188279176188280GA54GENICheterozygous112319236