chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	80257259	80257260	G	T	17	GENIC	homozygous	116063628
11	80260646	80260647	C	T	12	GENIC	homozygous	116063630
11	80264465	80264466	C	G	22	GENIC	homozygous	116063632
11	80265068	80265069	G	A	17	GENIC	homozygous	116063634
11	80266124	80266124		T	11	GENIC	possibly homozygous	132157352
11	80267752	80267753	G	C	20	GENIC	homozygous	115995701
11	80267838	80267839	C	G	11	GENIC	homozygous	132163419
11	80267840	80267841	C	G	11	GENIC	homozygous	118196080
11	80268362	80268363	C	T	28	GENIC	homozygous	115995703
11	80269228	80269229	T	G	19	GENIC	homozygous	115995705
11	80269232	80269233	T	A	21	GENIC	homozygous	115995707
11	80270144	80270145	C	T	23	GENIC	homozygous	115995709
11	80274234	80274238	TGTT		17	GENIC	homozygous	131482080
11	80275184	80275185	C		8	GENIC	homozygous	128926747
11	80275120	80275120		AA	12	GENIC	homozygous	128926742
11	80275132	80275132		G	11	GENIC	homozygous	128926743
11	80275139	80275139		G	11	GENIC	homozygous	128926744
11	80275144	80275144		GT	11	GENIC	homozygous	128926745
11	80275171	80275171		GG	10	GENIC	homozygous	128926746
11	80275190	80275191	T		7	GENIC	homozygous	128926748
11	80275233	80275233		G	5	GENIC	homozygous	128926749
11	80275241	80275241		G	5	GENIC	homozygous	128926750
11	80275246	80275247	A		5	GENIC	homozygous	128926751
11	80275483	80275485	CG		11	GENIC	homozygous	131109246
11	80275958	80275959	T	G	17	GENIC	homozygous	116063636
11	80276738	80276739	C	T	22	GENIC	homozygous	115995713
11	80276979	80276980	T	C	15	GENIC	homozygous	115995715
11	80277482	80277483	C	A	19	GENIC	homozygous	115995719
11	80277523	80277524	C	T	17	GENIC	homozygous	116063640
11	80278013	80278014	T	C	19	GENIC	homozygous	116063641
11	80279021	80279022	G	A	19	GENIC	homozygous	116063643
11	80275200	80275201	C	T	7	GENIC	homozygous	116298524