chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6108144351108144352CT30GENIChomozygous115150806
6108144879108144880GA31GENICpossibly homozygous115274142
6108145402108145403CG34GENIChomozygous115150810
6108146215108146216TA30GENIChomozygous115150811
6108146856108146857GC21GENIChomozygous115150812
6108147187108147188CT26GENIChomozygous115150813
6108147752108147753TA31GENIChomozygous115150814
6108147990108147991AG27GENIChomozygous115150815
6108148146108148147GT23GENIChomozygous115150816
6108148163108148164TC26GENIChomozygous115150817
6108148748108148749GA3GENIChomozygous115150818
6108149078108149079TC19GENIChomozygous115150819
6108149185108149186AT28GENIChomozygous115150820
6108149298108149299AG23GENIChomozygous115150821
6108149403108149404CT32GENIChomozygous115150822
6108149409108149410CA30GENIChomozygous115150823
6108149458108149459TA17GENIChomozygous115150824