chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	31976578	31976579	G	A	21	GENIC	homozygous	50349641
13	31979275	31979276	T	C	14	GENIC	homozygous	49705117
13	31981226	31981227	A	G	20	GENIC	homozygous	49705119
13	31982666	31982667	G	A	25	GENIC	homozygous	50349642
13	31982880	31982881	G	T	24	GENIC	homozygous	49705121
13	31983140	31983141	A	C	11	GENIC	heterozygous	49705122
13	31983846	31983847	A	T	23	GENIC	homozygous	49705124
13	31986303	31986304	T	C	20	GENIC	homozygous	49705128
13	31988453	31988454	G	A	12	GENIC	homozygous	50349643
13	31988665	31988683	CCATGCACTCCCTCCCCA	------------------	17	GENIC	homozygous	49705132
13	31988713	31988714	C	T	19	GENIC	homozygous	50349644
13	31988762	31988763	C	T	15	GENIC	homozygous	49922176
13	31988878	31988879	G	A	17	GENIC	homozygous	49922177
13	31988893	31988894	G	C	18	GENIC	homozygous	49922178
13	31988943	31988944	A	-	20	GENIC	possibly homozygous	50349645
13	31989254	31989255	A	G	21	GENIC	homozygous	49922180
13	31989474	31989475	A	G	21	GENIC	homozygous	49705136
13	31989542	31989543	G	GC	23	GENIC	homozygous	50349646
13	31989624	31989625	G	A	12	GENIC	homozygous	50349647
13	31990107	31990108	T	TA	13	GENIC	homozygous	50349648
13	31990191	31990192	T	C	13	GENIC	homozygous	50349649
13	31990226	31990227	T	C	16	GENIC	homozygous	50349650
13	31990277	31990278	G	C	15	GENIC	homozygous	50349651
13	31990974	31990975	G	A	22	GENIC	homozygous	50349652
13	31991012	31991013	G	GCA	19	GENIC	homozygous	50349653
13	31992431	31992432	G	A	11	GENIC	homozygous	50349654
13	31994761	31994762	T	-	16	GENIC	homozygous	49705158
13	31994936	31994937	A	G	24	GENIC	homozygous	50349656
13	31995859	31995860	C	A	13	GENIC	homozygous	49705163
13	31996266	31996267	A	G	12	GENIC	homozygous	49705164
13	31996607	31996608	C	A	23	GENIC	homozygous	49705166