chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130117240130117241CA20GENIChomozygous54110353
7130118246130118247T-11GENICheterozygous54110354
7130118274130118275CA15GENIChomozygous54110355
7130118914130118915AT7GENICheterozygous54754655
7130120300130120301AG10GENICpossibly homozygous54110356
7130120484130120485GT16GENIChomozygous54754659
7130120642130120643TC14GENIChomozygous54110360
7130121330130121331AG13GENIChomozygous54110361
7130121574130121575CT20GENIChomozygous54110363
7130121716130121717AG20GENICpossibly homozygous54110364
7130121749130121750AG17GENICpossibly homozygous54110365
7130123811130123812GA16GENICpossibly homozygous54754661
7130124254130124255GA12GENIChomozygous54754663
7130124264130124265TC11GENIChomozygous54110366