chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8131980042131980043GA9GENIChomozygous53066594
8131980127131980128AAT19GENIChomozygous53306553
8131980294131980295CT12GENIChomozygous53066595
8131981991131981992A-15GENIChomozygous53066597
8131982277131982278GA24GENIChomozygous53066598
8131982552131982553GGA16GENIChomozygous53306554
8131983919131983920TC16GENIChomozygous52900404
8131984045131984047CT--3GENIChomozygous53416146
8131984693131984694T-23GENIChomozygous52900410
8131985635131985641GCACAT------16GENIChomozygous52900418
8131985694131985695AG21GENIChomozygous53066600
8131986200131986201CT27GENIChomozygous53306556
8131986730131986731TC25GENIChomozygous52900430
8131986910131986911CCT22GENIChomozygous53066601
8131986947131986948CG20GENIChomozygous53066602
8131987092131987093AG30GENIChomozygous53066603
8131987200131987201AG29GENIChomozygous53066604
8131987352131987353GT33GENIChomozygous52900432
8131987559131987560GA30GENIChomozygous53066605
8131987639131987640GA27GENIChomozygous53066606
8131987650131987651CA20GENIChomozygous53066607
8131987708131987709AG19GENIChomozygous53066608
8131988002131988003TG20GENIChomozygous53066609
8131988274131988275AC20GENIChomozygous53066610
8131988296131988297TC23GENIChomozygous53066611
8131988654131988655TTTTAAGTAG30GENIChomozygous53066612
8131988849131988850AAT20GENIChomozygous53066613
8131989125131989126GT23GENIChomozygous53066614
8131989353131989354GA21GENIChomozygous53066615
8131989489131989490GA25GENIChomozygous53066616
8131989590131989591TC28GENIChomozygous53066617
8131989781131989782AT37GENIChomozygous53066618
8131990301131990302AAACTT31GENIChomozygous53066619
8131990357131990358CT22GENIChomozygous53066620
8131990473131990474TG26GENIChomozygous52900434
8131990701131990702TC31GENIChomozygous53066621
8131991741131991742TC33GENIChomozygous53066622