chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170262372	170262373	A	C	31	GENIC	homozygous	108375500
1	170262418	170262419	A	C	36	GENIC	homozygous	108375502
1	170262757	170262758	A	G	32	GENIC	homozygous	108375504
1	170262979	170262980	C	T	40	GENIC	homozygous	108375506
1	170263862	170263863	A	G	47	GENIC	homozygous	108375508
1	170264182	170264183	T	C	54	GENIC	homozygous	108375510
1	170264224	170264225	A	G	59	GENIC	homozygous	108375512
1	170264473	170264474	A	G	53	GENIC	homozygous	108375514
1	170264622	170264623	A	G	52	GENIC	homozygous	108375516
1	170265005	170265006	G	A	58	GENIC	homozygous	108375518
1	170265015	170265016	A	G	57	GENIC	homozygous	108375520
1	170265503	170265504	T	C	38	GENIC	homozygous	108375522
1	170265683	170265684	T	C	47	GENIC	homozygous	108375524
1	170265119	170265120	T		45	GENIC	homozygous	127455468
1	170265193	170265198	GACTA		51	GENIC	homozygous	127455469
1	170266684	170266686	CA		33	GENIC	homozygous	127455470
1	170266750	170266751	C	T	23	GENIC	homozygous	108375526
1	170266986	170266987	C	T	10	GENIC	homozygous	108375528
1	170267002	170267003	G	A	6	GENIC	homozygous	108375530
1	170267220	170267221	C	T	13	GENIC	homozygous	108375532
1	170267279	170267280	G	A	10	GENIC	possibly homozygous	108755101
1	170267885	170267886	G	A	32	GENIC	homozygous	108375536
1	170267919	170267920	A	G	38	GENIC	homozygous	108375538
1	170269227	170269228	T	C	46	GENIC	homozygous	108375540
1	170269278	170269279	T	G	37	GENIC	homozygous	108375542
1	170269659	170269660	G	A	38	GENIC	homozygous	108375544
1	170270944	170270945	T	C	48	GENIC	homozygous	108375546
1	170271310	170271311	C	G	42	GENIC	homozygous	108375548
1	170271689	170271690	A	G	33	GENIC	possibly homozygous	108375550
1	170272010	170272011	G	A	13	GENIC	homozygous	108375552