chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	37723669	37723670	C	G	26	GENIC	homozygous	51002531
11	37723848	37723849	C	G	27	GENIC	homozygous	51002532
11	37724182	37724184	TG	--	19	GENIC	possibly homozygous	50931288
11	37724303	37724304	A	ATG	22	GENIC	homozygous	50931292
11	37724337	37724338	A	G	24	GENIC	homozygous	50737212
11	37724344	37724346	TG	--	20	GENIC	homozygous	50737213
11	37724420	37724424	TGTG	----	20	GENIC	homozygous	51002533
11	37724530	37724540	TGTGTGTATA	----------	16	GENIC	homozygous	50737216
11	37724551	37724552	G	A	14	GENIC	homozygous	51002534
11	37725382	37725383	T	C	12	GENIC	homozygous	51002535
11	37725845	37725846	A	ATT	28	GENIC	homozygous	51002536
11	37725860	37725861	T	A	33	GENIC	homozygous	51160012
11	37726265	37726266	A	G	34	GENIC	homozygous	50737230
11	37726606	37726607	C	T	28	GENIC	homozygous	51002537
11	37726704	37726705	C	A	28	GENIC	homozygous	50737233
11	37726784	37726786	AA	--	22	GENIC	homozygous	51002538
11	37727243	37727244	C	T	14	GENIC	homozygous	51002541
11	37727956	37727957	C	CTT	3	GENIC	homozygous	51180435
11	37726040	37726041	T	C	20	GENIC	homozygous	51180432
11	37727937	37727938	T	TC	5	GENIC	homozygous	51180433
11	37727942	37727943	C	CTTCTTCTTCTTCT	5	GENIC	homozygous	51180434
11	37728163	37728164	T	TCTC	5	GENIC	heterozygous	51180436
11	37728252	37728253	A	G	20	GENIC	homozygous	51002542
11	37728568	37728569	A	G	15	GENIC	homozygous	50737252
11	37728584	37728586	AT	--	13	GENIC	homozygous	50878017
11	37729794	37729795	T	C	37	GENIC	homozygous	50737257
11	37730087	37730088	T	C	35	GENIC	homozygous	50737261
11	37730129	37730143	CCTGTGTGGTTTCT	--------------	42	GENIC	homozygous	51002543
11	37730334	37730335	C	T	27	GENIC	homozygous	51002544
11	37730628	37730629	T	TCCCCGGTCTGGAGACCCTTTCA	37	GENIC	homozygous	50737262
11	37730895	37730896	G	A	23	GENIC	homozygous	51002545
11	37730987	37730988	G	A	34	GENIC	homozygous	50737263
11	37731001	37731002	T	C	29	GENIC	homozygous	50737264
11	37731315	37731316	G	A	27	GENIC	homozygous	51002546
11	37731800	37731801	A	G	29	GENIC	homozygous	51002547