chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3974253 3974254 C T 17 GENIC homozygous 998997251 20 3975687 3975688 C G 13 GENIC homozygous 998997252 20 3975840 3975841 A G 13 GENIC homozygous 998997253 20 3976179 3976180 A G 35 GENIC homozygous 998997254 20 3976620 3976621 G T 19 GENIC homozygous 998997255 20 3976662 3976663 C T 23 GENIC homozygous 998997256 20 3976690 3976691 G A 25 GENIC homozygous 998997257 20 3976750 3976751 T A 28 GENIC homozygous 998997258 20 3976751 3976752 T C 28 GENIC homozygous 998997259 20 3976783 3976784 A C 26 GENIC homozygous 998997260 20 3976884 3976885 G A 25 GENIC homozygous 998997261 20 3976982 3976983 C A 34 GENIC homozygous 998997262 20 3976998 3976999 A G 34 GENIC homozygous 998997263 20 3977048 3977049 G A 28 GENIC homozygous 998997264 20 3977163 3977164 C T 22 GENIC homozygous 998997265 20 3977906 3977907 C T 24 GENIC homozygous 998997266 20 3978365 3978366 G A 12 GENIC homozygous 998997267