chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT12GENIChomozygous961070913
5159590355159590356AC39GENIChomozygous961070914
5159590356159590357GC39GENIChomozygous961070915
5159590377159590378GA34GENIChomozygous961070916
5159590516159590517AG30GENIChomozygous961070917
5159590543159590544TC23GENIChomozygous961070918
5159590567159590568TC23GENIChomozygous961070919
5159590810159590811GA30GENIChomozygous961070920
5159591041159591042CT22GENIChomozygous961070921
5159591165159591166AG28GENIChomozygous961070922
5159591294159591295GA28GENICpossibly homozygous961070923
5159591492159591493CT36GENIChomozygous961070924
5159591711159591712GA22GENIChomozygous961070925
5159591959159591960CT25GENIChomozygous961070926
5159592241159592242AG23GENIChomozygous961070927
5159592551159592552GA35GENIChomozygous961070928
5159592593159592594GA34GENIChomozygous961070929
5159592713159592714CT33GENIChomozygous961070930
5159593011159593012TA23GENIChomozygous961070931
5159593229159593230AG32GENIChomozygous961070932
5159593316159593317AC26GENIChomozygous961070933
5159594481159594482GA35GENIChomozygous961070934
5159595521159595522GA22GENIChomozygous961070935
5159598268159598269GA32GENIChomozygous961070936
5159599504159599505TC19GENIChomozygous961070937
5159600471159600472TC22GENIChomozygous961070938
5159601143159601144CT32GENIChomozygous961070939
5159601217159601218AG33GENIChomozygous961070940
5159601274159601275AG29GENIChomozygous961070941
5159602018159602019CT11GENIChomozygous961070942