chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136555182136555183TC37GENIChomozygous644474197
4136555204136555205GA36GENIChomozygous644474198
4136555931136555932CG32GENIChomozygous644474199
4136556846136556847CT28GENIChomozygous644474200
4136560889136560890CT25GENIChomozygous644474201
4136561038136561039CT30GENIChomozygous644474202
4136561898136561899CT23GENICpossibly homozygous644474203
4136563586136563587CT26GENICpossibly homozygous644474204
4136563866136563867CCT16GENICpossibly homozygous753756186
4136564182136564183CT20GENIChomozygous644474205
4136564595136564596GA17GENIChomozygous644474206
4136565358136565359TTAA16GENIChomozygous753756188
4136565412136565413GT25GENIChomozygous644474207
4136565535136565536GGGAA22GENIChomozygous753756189
4136566715136566716TC21GENIChomozygous644474208
4136566747136566748CT24GENIChomozygous644474209
4136567444136567445AG29GENIChomozygous644474210
4136568035136568036TC18GENIChomozygous644474211