chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31180070511800706TC41GENIChomozygous111448128
31180520811805209AG27GENIChomozygous112066220
31180634111806342AG36GENICpossibly homozygous111448134
31180881711808818TC32GENIChomozygous111448138
31181063211810633CT30GENIChomozygous112066222
31181132411811325CA20GENICpossibly homozygous111448140
31181153911811540TC28GENIChomozygous111448144