chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10543353	10543354	T	G	43	GENIC	homozygous	51616716
10	10543753	10543754	G	A	29	GENIC	homozygous	51616717
10	10543822	10543823	A	C	28	GENIC	homozygous	51616718
10	10544258	10544259	A	G	25	GENIC	homozygous	51324887
10	10545379	10545380	T	-	3	GENIC	homozygous	51324892
10	10545647	10545648	T	-	1	GENIC	homozygous	51324893
10	10545669	10545670	T	-	1	GENIC	homozygous	51324895
10	10545834	10545835	C	T	22	GENIC	homozygous	51616719
10	10546208	10546209	C	T	25	GENIC	homozygous	51616720
10	10546506	10546508	AC	--	20	GENIC	homozygous	51324896
10	10547648	10547649	C	T	22	GENIC	homozygous	51616721
10	10548836	10548837	T	A	11	GENIC	homozygous	51324900
10	10551973	10551974	A	G	37	GENIC	homozygous	51324903
10	10559416	10559417	G	A	30	GENIC	homozygous	51616723
10	10559510	10559511	G	GT	34	GENIC	homozygous	51616724
10	10560404	10560405	G	GTGTGCATGCACATGCACATGCACA	35	GENIC	homozygous	51324909
10	10560631	10560632	G	A	36	GENIC	homozygous	51616725