chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 110741872 110741873 T C 16 GENIC homozygous 939181156 13 110742696 110742697 A G 23 GENIC homozygous 939181157 13 110743778 110743779 C T 18 GENIC homozygous 939181158 13 110743788 110743789 C T 16 GENIC homozygous 939181159 13 110743858 110743859 G A 16 GENIC homozygous 939181160 13 110743981 110743982 T C 24 GENIC homozygous 939181161 13 110744513 110744514 A G 22 GENIC homozygous 939181162 13 110744526 110744527 C T 20 GENIC homozygous 939181163 13 110744864 110744865 C T 12 GENIC homozygous 939181164 13 110745556 110745557 A G 17 GENIC homozygous 939181165 13 110745588 110745589 A G 17 GENIC homozygous 939181166 13 110745907 110745908 T A 19 GENIC homozygous 939181167 13 110746508 110746509 C T 23 GENIC homozygous 939181168 13 110746797 110746798 C T 22 GENIC homozygous 939181169 13 110747171 110747172 T C 16 GENIC homozygous 939181170 13 110748032 110748033 A C 23 GENIC homozygous 939181171 13 110748585 110748586 C T 12 GENIC homozygous 939181172 13 110748713 110748714 T C 24 GENIC homozygous 939181173 13 110748723 110748724 T C 19 GENIC homozygous 939181174 13 110748906 110748907 A G 26 GENIC homozygous 939181175