chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	37724182	37724184	TG	--	26	GENIC	possibly homozygous	50931288
11	37724303	37724304	A	ATG	48	GENIC	homozygous	50931292
11	37724319	37724320	G	A	50	GENIC	possibly homozygous	51233029
11	37724448	37724450	TG	--	49	GENIC	possibly homozygous	50737214
11	37724521	37724522	A	ATG	16	GENIC	heterozygous	51212742
11	37725845	37725846	A	AT	15	GENIC	possibly homozygous	50737221
11	37725845	37725846	A	ATT	15	GENIC	heterozygous	51002536
11	37725857	37725858	T	TA	16	GENIC	heterozygous	50931295
11	37725860	37725861	T	A	19	GENIC	homozygous	51160012
11	37727705	37727706	C	T	22	GENIC	homozygous	50931300
11	37728163	37728164	T	TCTC	2	GENIC	homozygous	51180436
11	37728322	37728323	C	T	11	GENIC	possibly homozygous	50931306
11	37728568	37728569	A	G	23	GENIC	homozygous	50737252
11	37728584	37728585	A	T	22	GENIC	homozygous	51260091
11	37729185	37729186	C	A	22	GENIC	possibly homozygous	50931309
11	37729687	37729688	T	C	35	GENIC	possibly homozygous	50931313
11	37730087	37730088	T	C	29	GENIC	homozygous	50737261
11	37730528	37730529	C	T	23	GENIC	homozygous	50931316
11	37730628	37730629	T	TCCCCGGTCTGGAGACCCTTTCA	23	GENIC	homozygous	50737262
11	37730987	37730988	G	A	21	GENIC	homozygous	50737263
11	37731001	37731002	T	C	20	GENIC	homozygous	50737264
11	37731190	37731191	G	T	22	GENIC	homozygous	50931319
11	37731354	37731355	C	T	18	GENIC	homozygous	50737265
11	37731421	37731422	C	T	29	GENIC	homozygous	50931322
11	37731704	37731705	G	C	27	GENIC	possibly homozygous	50737266
11	37731714	37731715	G	A	25	GENIC	possibly homozygous	50931325