chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151873818718738188CT32GENIChomozygous65044776
151873907918739080CT22GENIChomozygous65044779
151873908318739084TC22GENICpossibly homozygous65044782
151873985618739857CG20GENICpossibly homozygous65044785
151874039318740394AG41GENICpossibly homozygous65044788
151874083318740834AG31GENIChomozygous65044791
151874156718741568AG31GENIChomozygous65044794