chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41601289	41601290	G	A	32	GENIC	homozygous	115426996
12	41601454	41601454		GT	18	GENIC	homozygous	131118622
12	41601460	41601461	A	G	18	GENIC	homozygous	115330907
12	41602176	41602176		TTAATTAG	40	GENIC	homozygous	131118623
12	41602862	41602863	G	A	45	GENIC	homozygous	115426998
12	41602878	41602879	G	A	41	GENIC	homozygous	115330909
12	41603124	41603125	T	A	57	GENIC	homozygous	115330911
12	41603149	41603150	G	A	56	GENIC	homozygous	115330913
12	41603683	41603694	GGTGTGCACTA		35	GENIC	homozygous	128990827
12	41603712	41603713	G	A	42	GENIC	homozygous	115330915
12	41603767	41603768	A	G	41	GENIC	homozygous	115330917
12	41606681	41606682	C	T	35	GENIC	homozygous	115330921
12	41608766	41608767	G	A	49	GENIC	homozygous	115330923
12	41609663	41609664	T	C	54	GENIC	homozygous	115330927
12	41609736	41609737	T	C	48	GENIC	homozygous	115330929
12	41609996	41609997	G	T	47	GENIC	possibly homozygous	115330931
12	41611680	41611681	C	T	33	GENIC	possibly homozygous	115427000
12	41615806	41615807	C	T	55	GENIC	homozygous	115427002
12	41616953	41616954	T	C	36	GENIC	homozygous	115330935
12	41618446	41618447	G	A	34	GENIC	homozygous	115427004
12	41618554	41618555	A	G	35	GENIC	homozygous	115330939