chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170262372	170262373	A	C	32	GENIC	homozygous	108375500
1	170262418	170262419	A	C	28	GENIC	homozygous	108375502
1	170262757	170262758	A	G	26	GENIC	homozygous	108375504
1	170262979	170262980	C	T	15	GENIC	homozygous	108375506
1	170263862	170263863	A	G	17	GENIC	homozygous	108375508
1	170264182	170264183	T	C	17	GENIC	homozygous	108375510
1	170264224	170264225	A	G	19	GENIC	possibly homozygous	108375512
1	170264473	170264474	A	G	9	GENIC	homozygous	108375514
1	170264622	170264623	A	G	11	GENIC	homozygous	108375516
1	170264777	170264778	G	A	11	GENIC	homozygous	108755099
1	170265005	170265006	G	A	17	GENIC	possibly homozygous	108375518
1	170265015	170265016	A	G	16	GENIC	homozygous	108375520
1	170265503	170265504	T	C	17	GENIC	homozygous	108375522
1	170265683	170265684	T	C	30	GENIC	homozygous	108375524
1	170266750	170266751	C	T	23	GENIC	homozygous	108375526
1	170266986	170266987	C	T	14	GENIC	homozygous	108375528
1	170267002	170267003	G	A	11	GENIC	homozygous	108375530
1	170267220	170267221	C	T	22	GENIC	possibly homozygous	108375532
1	170267277	170267278	G	A	27	GENIC	heterozygous	108755100
1	170267279	170267280	G	A	27	GENIC	heterozygous	108755101
1	170267281	170267282	G	A	28	GENIC	heterozygous	108755103
1	170267581	170267582	A	T	2	GENIC	homozygous	109437508
1	170267885	170267886	G	A	19	GENIC	homozygous	108375536
1	170267919	170267920	A	G	17	GENIC	homozygous	108375538
1	170269227	170269228	T	C	27	GENIC	homozygous	108375540
1	170269278	170269279	T	G	16	GENIC	homozygous	108375542
1	170269659	170269660	G	A	30	GENIC	homozygous	108375544
1	170270944	170270945	T	C	30	GENIC	homozygous	108375546
1	170271310	170271311	C	G	31	GENIC	homozygous	108375548
1	170271689	170271690	A	G	16	GENIC	homozygous	108375550
1	170272010	170272011	G	A	20	GENIC	homozygous	108375552