chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 38105003 38105004 C T 21 GENIC heterozygous 822919194 8 38105020 38105021 A T 18 GENIC heterozygous 822919195 8 38105069 38105070 T A 10 GENIC heterozygous 822919196 8 38105095 38105096 C T 12 GENIC heterozygous 822919197 8 38105105 38105106 T C 11 GENIC heterozygous 822919198 8 38105109 38105110 A C 11 GENIC heterozygous 822919199 8 38105173 38105174 G A 16 GENIC heterozygous 822919200 8 38105372 38105373 T C 16 GENIC heterozygous 822919201 8 38105377 38105378 A G 22 GENIC heterozygous 822919202 8 38105389 38105390 T C 21 GENIC heterozygous 822919203 8 38105479 38105480 G A 29 GENIC heterozygous 822919204 8 38105487 38105488 G A 30 GENIC heterozygous 822919205 8 38105697 38105698 G C 24 GENIC heterozygous 822919206 8 38105751 38105752 A C 25 GENIC heterozygous 822919207 8 38105753 38105754 T G 25 GENIC heterozygous 822919208 8 38105759 38105760 A G 27 GENIC heterozygous 822919209 8 38105788 38105789 C T 30 GENIC heterozygous 822919210 8 38105835 38105836 G A 31 GENIC heterozygous 822919211 8 38105858 38105859 G A 33 GENIC heterozygous 822919212 8 38105881 38105882 G A 27 GENIC heterozygous 822919213 8 38105890 38105891 T C 28 GENIC heterozygous 822919214 8 38105981 38105982 C T 18 GENIC heterozygous 822919215 8 38105996 38105997 C T 17 GENIC heterozygous 822919216