chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36117018	36117019	A	G	13	GENIC	homozygous	51411863
10	36117052	36117053	T	C	15	GENIC	homozygous	51411865
10	36117093	36117094	T	C	16	GENIC	homozygous	51411867
10	36117412	36117413	G	T	9	GENIC	homozygous	51411873
10	36117690	36117691	A	-	10	GENIC	homozygous	51411875
10	36120372	36120373	A	G	10	GENIC	homozygous	51411879
10	36120775	36120776	T	G	8	GENIC	homozygous	53558614
10	36121674	36121675	A	G	13	GENIC	homozygous	51411885
10	36121700	36121701	G	A	10	GENIC	homozygous	51411887
10	36121701	36121702	G	GTA	10	GENIC	homozygous	51411889
10	36123867	36123869	GG	--	9	GENIC	homozygous	51411899
10	36123871	36123872	G	GACA	10	GENIC	homozygous	51411901
10	36123877	36123878	C	T	11	GENIC	homozygous	51411903
10	36123933	36123934	C	T	16	GENIC	homozygous	51411905
10	36123979	36123980	A	G	13	GENIC	homozygous	51411907
10	36123986	36123987	A	G	14	GENIC	homozygous	51411909
10	36123990	36123991	C	T	13	GENIC	homozygous	51411911
10	36124007	36124008	C	T	15	GENIC	homozygous	51411913
10	36125812	36125813	C	A	9	GENIC	heterozygous	51411917
10	36127308	36127309	T	TCC	6	GENIC	heterozygous	51411925
10	36128067	36128068	C	T	11	GENIC	heterozygous	51411929
10	36128358	36128359	T	C	15	GENIC	heterozygous	52138949
10	36129008	36129009	T	A	16	GENIC	heterozygous	51411933
10	36130691	36130692	A	T	13	GENIC	homozygous	51411937
10	36130834	36130835	A	G	10	GENIC	homozygous	51411939
10	36131584	36131585	C	CCCT	7	GENIC	homozygous	51411951
10	36131642	36131643	C	T	13	GENIC	homozygous	51411953
10	36132273	36132274	C	T	16	GENIC	homozygous	51411955
10	36132816	36132817	C	T	20	GENIC	heterozygous	52138961
10	36132872	36132873	C	T	15	GENIC	heterozygous	51411959
10	36132982	36132983	T	-	16	GENIC	heterozygous	51411961
10	36133305	36133306	T	G	12	GENIC	heterozygous	52138963
10	36128247	36128248	C	-	9	GENIC	heterozygous	51984751