chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8131979947131979948A-3GENICheterozygous53172685
8131980042131980043GA19GENIChomozygous53066594
8131980127131980128AAT18GENIChomozygous53306553
8131980294131980295CT17GENIChomozygous53066595
8131981991131981992A-15GENIChomozygous53066597
8131982277131982278GA42GENIChomozygous53066598
8131982552131982553GGA18GENIChomozygous53306554
8131983919131983920TC48GENIChomozygous52900404
8131984041131984047CTCTCT------7GENICheterozygous53563978
8131984045131984047CT--7GENICheterozygous53416146
8131984693131984694T-24GENIChomozygous52900410
8131985564131985590CACACACACACACACACACACACACA--------------------------4GENICheterozygous53416147
8131985635131985641GCACAT------17GENIChomozygous52900418
8131985694131985695AG28GENIChomozygous53066600
8131986200131986201CT48GENIChomozygous53306556
8131986730131986731TC33GENIChomozygous52900430
8131986910131986911CCT35GENIChomozygous53066601
8131986947131986948CG37GENIChomozygous53066602
8131987092131987093AG41GENIChomozygous53066603
8131987200131987201AG41GENIChomozygous53066604
8131987352131987353GT32GENIChomozygous52900432
8131987559131987560GA34GENIChomozygous53066605
8131987639131987640GA38GENIChomozygous53066606
8131987650131987651CA35GENIChomozygous53066607
8131987708131987709AG49GENIChomozygous53066608
8131988002131988003TG24GENIChomozygous53066609
8131988274131988275AC24GENIChomozygous53066610
8131988296131988297TC24GENIChomozygous53066611
8131988654131988655TTTTAAGTAG40GENIChomozygous53066612
8131988849131988850AAT37GENIChomozygous53066613
8131989125131989126GT39GENIChomozygous53066614
8131989353131989354GA29GENIChomozygous53066615
8131989489131989490GA23GENIChomozygous53066616
8131989590131989591TC24GENIChomozygous53066617
8131989781131989782AT36GENIChomozygous53066618
8131990301131990302AAACTT33GENIChomozygous53066619
8131990357131990358CT33GENIChomozygous53066620
8131990473131990474TG48GENIChomozygous52900434
8131990701131990702TC26GENIChomozygous53066621
8131991741131991742TC39GENIChomozygous53066622