chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	37346035	37346036	C	T	14	GENIC	homozygous	55232470
6	37346047	37346048	G	C	15	GENIC	homozygous	55232472
6	37346712	37346722	GCCTCCTAGA	----------	30	GENIC	homozygous	55232476
6	37347013	37347014	C	T	27	GENIC	homozygous	55232478
6	37347361	37347362	C	T	31	GENIC	homozygous	55232480
6	37347728	37347729	A	G	38	GENIC	homozygous	55232482
6	37349724	37349725	G	A	22	GENIC	homozygous	55232486
6	37349958	37349959	A	G	31	GENIC	homozygous	55232488
6	37350193	37350194	G	A	23	GENIC	homozygous	55232490
6	37350303	37350304	G	T	24	GENIC	homozygous	55232492
6	37350829	37350830	G	A	24	GENIC	homozygous	55232494
6	37351574	37351575	T	C	43	GENIC	homozygous	55232496
6	37351909	37351910	T	C	23	GENIC	homozygous	55232498
6	37352022	37352023	A	T	22	GENIC	homozygous	55232500
6	37352137	37352138	T	TC	15	GENIC	homozygous	54354169
6	37352202	37352205	GGG	---	14	GENIC	homozygous	55232504
6	37354150	37354151	T	C	28	GENIC	homozygous	55232510
6	37349254	37349258	ACAC	----	11	GENIC	heterozygous	54865730
6	37349256	37349258	AC	--	11	GENIC	possibly homozygous	55700198
6	37350035	37350036	C	T	26	GENIC	homozygous	55700200
6	37351093	37351094	A	T	18	GENIC	homozygous	55700202
6	37351095	37351096	G	A	18	GENIC	homozygous	55700204
6	37356363	37356364	A	AGT	10	GENIC	heterozygous	55232512
6	37356521	37356525	TTTT	----	29	GENIC	homozygous	55494462
6	37356524	37356525	T	TCCAA	27	GENIC	homozygous	55494464
6	37356363	37356364	A	AGTGTGT	10	GENIC	possibly homozygous	55648997