chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 104912966 104912967 C T 10 GENIC heterozygous 120097146 X 104912974 104912975 C T 10 GENIC heterozygous 120097147 X 104913003 104913004 A G 8 GENIC heterozygous 119942613 X 104913009 104913010 G T 8 GENIC heterozygous 119942614 X 104913026 104913027 G C 8 GENIC heterozygous 120707185 X 104913028 104913029 C T 8 GENIC heterozygous 120707186 X 104927242 104927243 A G 10 GENIC homozygous 120707188 X 104927325 104927326 T A 10 GENIC homozygous 108307893 X 104927326 104927327 A C 10 GENIC homozygous 108307895 X 104927339 104927340 T C 11 GENIC homozygous 108307897 X 104926063 104926064 G T 6 GENIC homozygous 108409777 X 104926065 104926066 G T 6 GENIC homozygous 108409779