chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 31146243 31146245 CG 28 GENIC homozygous 128980748 12 31146271 31146271 C 26 GENIC homozygous 128980749 12 31146331 31146332 T 23 GENIC homozygous 128980750 12 31146360 31146363 CTG 17 GENIC homozygous 128980751 12 31146390 31146391 A 17 GENIC homozygous 128980752 12 31146422 31146422 G 15 GENIC homozygous 128980753 12 31146452 31146452 C 13 GENIC homozygous 128980754 12 31146578 31146579 T 30 GENIC homozygous 128980755 12 31146625 31146626 G 35 GENIC homozygous 128980756 12 31146673 31146674 T 33 GENIC homozygous 128980757 12 31146713 31146714 C 26 GENIC homozygous 128980758 12 31146728 31146728 C 25 GENIC homozygous 128980759 12 31146831 31146831 T 17 GENIC homozygous 128980760 12 31146838 31146839 G 17 GENIC homozygous 128980761 12 31146854 31146855 G 17 GENIC homozygous 128980762 12 31146884 31146885 G 15 GENIC homozygous 128980763 12 31146889 31146890 T 14 GENIC homozygous 128980764 12 31146907 31146908 A 14 GENIC homozygous 128980765 12 31146912 31146913 G 14 GENIC homozygous 128980766 12 31146936 31146936 T 13 GENIC homozygous 128980767 12 31146980 31146981 C 12 GENIC homozygous 128980768 12 31147012 31147012 C 12 GENIC homozygous 128980769 12 31147034 31147034 T 12 GENIC homozygous 128980770 12 31152220 31152221 G 6 GENIC homozygous 128980773