chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6144512667144512668CT25GENIChomozygous628247357
6144512950144512951GA37GENIChomozygous628247358
6144514714144514715AG46GENIChomozygous628247359
6144515833144515834TC45GENIChomozygous628247360
6144516170144516171AG14GENIChomozygous628247361
6144518272144518273AT23GENIChomozygous628247362
6144518417144518418CCG15GENIChomozygous744422018
6144518607144518608GT30GENIChomozygous628247363
6144518869144518870CA22GENIChomozygous628247364
6144520045144520046AT18GENIChomozygous628247365
6144520062144520063CT24GENIChomozygous628247366
6144520151144520152TC23GENIChomozygous628247367
6144520363144520364CG29GENICpossibly homozygous628247368
6144520499144520502CCC---6GENIChomozygous744422019
6144520883144520884CCA23GENIChomozygous744422020
6144520887144520888CCT25GENIChomozygous744422021
6144520916144520917GA23GENIChomozygous628247369
6144523159144523160TTG1GENIChomozygous744422022
6144523383144523384TC9GENIChomozygous628247370