chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80257259	80257260	G	T	16	GENIC	homozygous	116063628
11	80260646	80260647	C	T	25	GENIC	homozygous	116063630
11	80264465	80264466	C	G	25	GENIC	homozygous	116063632
11	80265068	80265069	G	A	23	GENIC	homozygous	116063634
11	80267752	80267753	G	C	21	GENIC	homozygous	115995701
11	80267840	80267841	C	G	19	GENIC	heterozygous	118196080
11	80267842	80267843	C	G	20	GENIC	heterozygous	118196081
11	80268362	80268363	C	T	25	GENIC	homozygous	115995703
11	80269228	80269229	T	G	28	GENIC	homozygous	115995705
11	80269232	80269233	T	A	27	GENIC	homozygous	115995707
11	80270144	80270145	C	T	18	GENIC	homozygous	115995709
11	80275200	80275201	C	T	14	GENIC	homozygous	116298524
11	80275958	80275959	T	G	22	GENIC	homozygous	116063636
11	80276004	80276005	T	C	20	GENIC	homozygous	116063638
11	80276738	80276739	C	T	16	GENIC	homozygous	115995713
11	80276979	80276980	T	C	22	GENIC	homozygous	115995715
11	80277482	80277483	C	A	23	GENIC	homozygous	115995719
11	80277523	80277524	C	T	22	GENIC	homozygous	116063640
11	80278013	80278014	T	C	12	GENIC	homozygous	116063641
11	80279021	80279022	G	A	24	GENIC	homozygous	116063643