chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	30857066	30857067	T	G	41	GENIC	possibly homozygous	108711835
1	30857628	30857629	G	T	50	GENIC	possibly homozygous	108711837
1	30858765	30858766	T	C	34	GENIC	possibly homozygous	108711839
1	30859578	30859579	A	G	62	GENIC	homozygous	108711841
1	30859621	30859622	G	A	76	GENIC	possibly homozygous	108711843
1	30860161	30860162	A	G	86	GENIC	homozygous	108711845
1	30861828	30861829	A	G	73	GENIC	homozygous	108711847
1	30861895	30861896	A	T	56	GENIC	homozygous	108711849
1	30862062	30862063	G	A	74	GENIC	homozygous	108711851
1	30863058	30863059	A	C	74	GENIC	possibly homozygous	108711853
1	30864752	30864753	G	A	77	GENIC	homozygous	108711855
1	30865477	30865478	C	A	39	GENIC	homozygous	108066582
1	30865482	30865483	C	G	34	GENIC	possibly homozygous	108711857
1	30865485	30865486	G	T	33	GENIC	possibly homozygous	108711859
1	30865900	30865901	C	T	61	GENIC	homozygous	108711861
1	30868907	30868908	T	A	65	GENIC	homozygous	108066583
1	30869139	30869140	G	A	58	GENIC	homozygous	108711863
1	30870719	30870720	T	A	81	GENIC	homozygous	108711865
1	30872451	30872452	C	T	60	GENIC	homozygous	108711867