chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 19382908 19382909 A T 11 GENIC homozygous 50098909 12 19383144 19383154 GTGTGTGTGT ---------- 2 GENIC homozygous 50536722 12 19383277 19383281 TTTT ---- 11 GENIC homozygous 50284575 12 19383292 19383293 T G 13 GENIC homozygous 50536724 12 19383394 19383395 A G 12 GENIC homozygous 50098915 12 19383632 19383633 T C 18 GENIC homozygous 50098917 12 19384278 19384279 A AT 10 GENIC heterozygous 50483202 12 19384279 19384280 T - 10 GENIC heterozygous 50098919 12 19384710 19384711 A ATGTG 1 GENIC homozygous 50536726 12 19384747 19384748 G T 6 GENIC homozygous 50483206 12 19387032 19387033 T C 10 GENIC homozygous 50098935 12 19387195 19387196 G GGTGTGT 8 GENIC possibly homozygous 50536730 12 19387195 19387196 G GGTGTGTGT 8 GENIC heterozygous 50536732 12 19387896 19387897 G GCATCTC 3 GENIC homozygous 50098939 12 19388323 19388324 G T 9 GENIC homozygous 50368775 12 19388722 19388723 G A 20 GENIC homozygous 50483208 12 19389102 19389103 T C 17 GENIC homozygous 50098941 12 19389126 19389127 T C 17 GENIC homozygous 50098943 12 19390611 19390612 A G 12 GENIC homozygous 50098945 12 19390920 19390921 C A 12 GENIC homozygous 50483210 12 19390999 19391000 T C 19 GENIC homozygous 50098947