chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	101057591	101057592	G	A	33	GENIC	heterozygous	61732181
1	101057596	101057597	T	C	32	GENIC	heterozygous	61732183
1	101057612	101057613	G	A	30	GENIC	heterozygous	61732185
1	101057820	101057821	T	G	25	GENIC	heterozygous	61483998
1	101057848	101057849	A	G	25	GENIC	heterozygous	61483999
1	101057851	101057852	T	C	24	GENIC	heterozygous	61484000
1	101057856	101057857	T	G	23	GENIC	heterozygous	61484001
1	101057864	101057865	G	C	25	GENIC	heterozygous	60779710
1	101057942	101057943	C	G	31	GENIC	heterozygous	60779711
1	101057964	101057965	A	AC	33	GENIC	heterozygous	60779712
1	101058033	101058034	A	T	34	GENIC	heterozygous	60779713
1	101058043	101058044	G	A	31	GENIC	heterozygous	60779714
1	101058078	101058079	A	-	24	GENIC	heterozygous	60779715
1	101058095	101058096	A	T	29	GENIC	heterozygous	60779716
1	101058103	101058104	C	A	34	GENIC	heterozygous	61953329
1	101058452	101058453	A	G	8	GENIC	heterozygous	61953330
1	101058536	101058538	AC	--	3	GENIC	homozygous	60779717
1	101058689	101058690	A	AAG	12	GENIC	heterozygous	61484006
1	101058689	101058690	A	AAGAG	12	GENIC	possibly homozygous	61484007
1	101058927	101058928	C	A	25	GENIC	heterozygous	60779718
1	101058981	101058982	C	A	30	GENIC	heterozygous	61892423
1	101063603	101063604	C	T	27	GENIC	heterozygous	61892424
1	101063606	101063607	C	T	28	GENIC	heterozygous	60779719
1	101063627	101063628	A	G	30	GENIC	heterozygous	60779720
1	101063642	101063643	G	T	30	GENIC	heterozygous	60779721