chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106974786106974787CT29GENIChomozygous534245628
10106975785106975786TTCC44GENIChomozygous696089617
10106976030106976031CA32GENICpossibly homozygous536915727
10106976031106976032AC31GENIChomozygous536915728
10106984727106984729TA--33GENICheterozygous696089618
10106993451106993452A-9GENICheterozygous696089621
10107002263107002269ATGAAT------38GENICheterozygous696089622