chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10543428	10543429	G	A	26	GENIC	homozygous	51804298
10	10544258	10544259	A	G	13	GENIC	homozygous	51324887
10	10544464	10544465	C	T	26	GENIC	homozygous	51804300
10	10545213	10545214	G	-	12	GENIC	homozygous	51804302
10	10545379	10545380	T	-	1	GENIC	homozygous	51324892
10	10545647	10545648	T	-	6	GENIC	homozygous	51324893
10	10545934	10545935	A	G	30	GENIC	homozygous	51804304
10	10546506	10546508	AC	--	26	GENIC	homozygous	51324896
10	10546543	10546544	A	G	36	GENIC	possibly homozygous	51804306
10	10546830	10546831	C	T	34	GENIC	homozygous	51804308
10	10547079	10547080	C	T	30	GENIC	homozygous	51804310
10	10547269	10547270	A	C	22	GENIC	homozygous	51324897
10	10548286	10548287	A	G	29	GENIC	homozygous	51804312
10	10548464	10548465	G	T	27	GENIC	homozygous	51804314
10	10548836	10548837	T	A	9	GENIC	homozygous	51324900
10	10550634	10550635	G	A	25	GENIC	homozygous	51804316
10	10551594	10551595	T	G	32	GENIC	homozygous	51324902
10	10551973	10551974	A	G	35	GENIC	homozygous	51324903
10	10552383	10552384	A	G	35	GENIC	homozygous	51804318
10	10552907	10552908	C	T	35	GENIC	homozygous	51804320
10	10553110	10553111	G	A	24	GENIC	homozygous	51804322
10	10553254	10553255	C	T	11	GENIC	homozygous	51804324
10	10554255	10554256	C	T	13	GENIC	homozygous	51804326
10	10555788	10555789	A	G	32	GENIC	homozygous	51804328
10	10556593	10556594	G	A	38	GENIC	homozygous	51804330
10	10556971	10556972	A	G	33	GENIC	homozygous	51324905
10	10557208	10557209	A	G	35	GENIC	homozygous	51324906
10	10558153	10558154	C	T	28	GENIC	homozygous	51804332
10	10559060	10559061	A	G	52	GENIC	homozygous	51324907
10	10559458	10559459	C	T	30	GENIC	homozygous	51804334
10	10560404	10560405	G	GTGTGCATGCACATGCACATGCACA	41	GENIC	homozygous	51324909
10	10563011	10563012	G	A	32	GENIC	homozygous	51804336