chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10544258	10544259	A	G	34	GENIC	homozygous	51324887
10	10544345	10544346	G	T	23	GENIC	homozygous	51324888
10	10544683	10544687	TATT	----	32	GENIC	homozygous	51324889
10	10544789	10544790	G	A	43	GENIC	homozygous	51324890
10	10545379	10545380	T	-	4	GENIC	homozygous	51324892
10	10545668	10545669	C	-	15	GENIC	heterozygous	51324894
10	10545669	10545670	T	-	5	GENIC	heterozygous	51324895
10	10546506	10546508	AC	--	33	GENIC	homozygous	51324896
10	10547269	10547270	A	C	30	GENIC	homozygous	51324897
10	10548179	10548180	G	A	31	GENIC	homozygous	51324898
10	10548818	10548819	C	T	23	GENIC	possibly homozygous	51324899
10	10548836	10548837	T	A	26	GENIC	homozygous	51324900
10	10549415	10549416	A	G	31	GENIC	homozygous	51324901
10	10551594	10551595	T	G	43	GENIC	homozygous	51324902
10	10551973	10551974	A	G	38	GENIC	homozygous	51324903
10	10555864	10555865	C	T	47	GENIC	homozygous	51324904
10	10556971	10556972	A	G	32	GENIC	homozygous	51324905
10	10557208	10557209	A	G	29	GENIC	homozygous	51324906
10	10559060	10559061	A	G	37	GENIC	homozygous	51324907
10	10560108	10560110	TG	--	22	GENIC	homozygous	51324908
10	10560404	10560405	G	GTGTGCATGCACATGCACATGCACA	16	GENIC	homozygous	51324909