chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11039743	11039744	T	A	26	GENIC	possibly homozygous	47018712
17	11040647	11040648	G	A	22	GENIC	possibly homozygous	48072841
17	11041614	11041615	T	C	33	GENIC	possibly homozygous	47018715
17	11041847	11041848	G	A	33	GENIC	possibly homozygous	48072842
17	11041967	11041968	G	A	29	GENIC	homozygous	48072843
17	11042477	11042478	T	C	24	GENIC	homozygous	48072844
17	11043100	11043101	G	A	23	GENIC	homozygous	48072845
17	11043496	11043497	A	AG	7	GENIC	homozygous	47702834
17	11044447	11044448	G	C	20	GENIC	possibly homozygous	47018718
17	11045305	11045306	A	T	26	GENIC	homozygous	47018719
17	11045306	11045307	A	T	27	GENIC	homozygous	47018720
17	11045725	11045726	A	G	36	GENIC	homozygous	47018721
17	11046174	11046175	T	C	31	GENIC	homozygous	48072846
17	11046819	11046820	C	T	25	GENIC	homozygous	48072847
17	11048988	11048989	C	G	31	GENIC	homozygous	47018723
17	11049629	11049631	GC	--	27	GENIC	homozygous	48072848
17	11049669	11049670	T	C	23	GENIC	homozygous	47018724