chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	90603045	90603046	T	C	32	GENIC	homozygous	50863905
11	90603082	90603083	C	T	42	GENIC	homozygous	50863906
11	90603153	90603154	A	AT	48	GENIC	homozygous	50863907
11	90603155	90603156	A	C	54	GENIC	homozygous	51135330
11	90603156	90603157	G	A	55	GENIC	homozygous	51171277
11	90603798	90603799	C	T	31	GENIC	homozygous	51135333
11	90604733	90604734	A	G	27	GENIC	homozygous	50863909
11	90605064	90605065	G	A	37	GENIC	homozygous	50863910
11	90605226	90605227	C	T	41	GENIC	homozygous	50863911
11	90605480	90605481	G	A	31	GENIC	homozygous	50863913
11	90605516	90605517	C	T	28	GENIC	homozygous	50863914
11	90605579	90605580	T	C	22	GENIC	homozygous	50863915
11	90606001	90606002	A	G	31	GENIC	homozygous	50863916
11	90606109	90606110	G	A	45	GENIC	homozygous	50974886
11	90606282	90606283	G	A	45	GENIC	homozygous	50863918
11	90606729	90606730	G	A	31	GENIC	homozygous	51135336