chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	42489900	42489901	A	G	38	GENIC	homozygous	112493636
15	42490697	42490698	C	T	29	GENIC	homozygous	112673114
15	42490882	42490883	T	G	46	GENIC	homozygous	112493638
15	42491180	42491181	A	G	32	GENIC	homozygous	112493640
15	42491288	42491289	C	T	34	GENIC	possibly homozygous	112493642
15	42491299	42491300	T	C	32	GENIC	homozygous	112493644
15	42491594	42491595	G	A	37	GENIC	homozygous	112493646
15	42491690	42491691	T	C	49	GENIC	homozygous	112493650
15	42492819	42492820	A	T	56	GENIC	homozygous	112493652
15	42492820	42492821	A	T	58	GENIC	homozygous	112493654
15	42492838	42492839	T	C	66	GENIC	homozygous	112493656
15	42492958	42492959	C	T	43	GENIC	homozygous	112493658
15	42492989	42492990	T	C	37	GENIC	homozygous	112493660
15	42493048	42493049	A	G	35	GENIC	homozygous	112493662
15	42493344	42493345	A	C	45	GENIC	homozygous	112493664
15	42497655	42497656	A	G	49	GENIC	homozygous	112493678
15	42497940	42497941	G	A	48	GENIC	homozygous	112673116
15	42498804	42498805	T	G	46	GENIC	homozygous	112673118
15	42500335	42500336	G	A	51	GENIC	homozygous	112673120