chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139705479139705480TC20GENIChomozygous115937178
7139705495139705496AG23GENIChomozygous115937179
7139708221139708222CT31GENIChomozygous115937180
7139710471139710472GC22GENIChomozygous115937181
7139710760139710761AG25GENIChomozygous115937182
7139711273139711274AG29GENIChomozygous115937183
7139711292139711293TC24GENIChomozygous115937184
7139711738139711739AG40GENIChomozygous115937185
7139712075139712076GA27GENIChomozygous115937186
7139712397139712398CT37GENIChomozygous115937187
7139715727139715728CT23GENIChomozygous115937188
7139716287139716288TC53GENICheterozygous116377770
7139716392139716393GA37GENIChomozygous115937189
7139716795139716796GA56GENICheterozygous116377772
7139719779139719780TC22GENIChomozygous115937191