chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	90603045	90603046	T	C	18	GENIC	homozygous	50863905
11	90603082	90603083	C	T	25	GENIC	homozygous	50863906
11	90603153	90603154	A	AT	34	GENIC	homozygous	50863907
11	90603155	90603156	A	C	35	GENIC	homozygous	51135330
11	90603156	90603157	G	A	35	GENIC	homozygous	51171277
11	90603857	90603858	G	C	24	GENIC	homozygous	50863908
11	90604733	90604734	A	G	18	GENIC	homozygous	50863909
11	90605064	90605065	G	A	22	GENIC	homozygous	50863910
11	90605226	90605227	C	T	19	GENIC	homozygous	50863911
11	90605326	90605327	G	T	26	GENIC	homozygous	50863912
11	90605480	90605481	G	A	23	GENIC	homozygous	50863913
11	90605516	90605517	C	T	16	GENIC	homozygous	50863914
11	90605579	90605580	T	C	18	GENIC	homozygous	50863915
11	90606001	90606002	A	G	27	GENIC	homozygous	50863916
11	90606066	90606067	G	A	21	GENIC	homozygous	50863917
11	90606282	90606283	G	A	37	GENIC	homozygous	50863918