chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100298250100298251CA9GENIChomozygous108898713
1100300919100300920CT28GENIChomozygous108898714
1100300960100300961GA28GENIChomozygous108898715
1100301038100301039CA27GENIChomozygous108898716
1100301667100301668CG18GENIChomozygous108898717
1100302723100302724CT25GENIChomozygous108898718
1100303806100303807GA25GENIChomozygous108898719
1100305076100305077CG17GENIChomozygous120514444
1100305784100305785CT34GENIChomozygous108898721
1100308983100308984GA32GENIChomozygous108898724
1100309925100309926AG30GENIChomozygous108898725
1100310625100310626CT36GENIChomozygous108898726
1100311791100311792GA29GENIChomozygous108898727
1100311867100311868CT28GENIChomozygous108898728
1100312188100312189GA27GENIChomozygous108898729
1100316501100316502AG25GENIChomozygous108898730
1100316866100316867TC22GENIChomozygous108898731
1100321396100321397TC28GENIChomozygous108898734
1100324978100324979TG25GENIChomozygous108898737
1100327047100327048AG21GENIChomozygous108898738
1100327154100327155AG19GENIChomozygous108898739
1100328687100328688CT23GENIChomozygous108898741
1100328822100328823TC19GENIChomozygous108898742
1100329817100329818CT21GENIChomozygous108898744
1100332339100332340AG25GENIChomozygous108898745
1100332497100332498GC20GENIChomozygous108898746
1100333961100333962GT21GENIChomozygous108898748
1100334055100334056AG31GENIChomozygous108898749
1100337058100337059TG22GENIChomozygous108898750