chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139705479139705480TC28GENIChomozygous115937178
7139705495139705496AG25GENIChomozygous115937179
7139708221139708222CT37GENIChomozygous115937180
7139710471139710472GC30GENIChomozygous115937181
7139710760139710761AG25GENIChomozygous115937182
7139711273139711274AG32GENIChomozygous115937183
7139711292139711293TC29GENIChomozygous115937184
7139711738139711739AG30GENIChomozygous115937185
7139712075139712076GA34GENIChomozygous115937186
7139712397139712398CT42GENIChomozygous115937187
7139716392139716393GA30GENIChomozygous115937189
7139719779139719780TC33GENIChomozygous115937191