chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170423607	170423608	C	G	45	GENIC	homozygous	108958821
1	170424009	170424010	C	T	48	GENIC	homozygous	108376018
1	170424784	170424785	C	T	42	GENIC	possibly homozygous	108376020
1	170424832	170424833	C	T	58	GENIC	homozygous	108958822
1	170424916	170424917	A	C	47	GENIC	homozygous	108376022
1	170425360	170425361	G	A	46	GENIC	homozygous	108376024
1	170425803	170425804	G	C	32	GENIC	homozygous	109052136
1	170426600	170426601	A	G	70	GENIC	possibly homozygous	108376030
1	170428771	170428772	A	G	57	GENIC	homozygous	108376038
1	170429010	170429011	C	G	59	GENIC	homozygous	108376040
1	170429203	170429204	T	G	60	GENIC	homozygous	108958823
1	170429419	170429420	C	T	46	GENIC	homozygous	108958824
1	170429519	170429520	A	T	50	GENIC	possibly homozygous	108958825
1	170429610	170429611	T	A	15	GENIC	possibly homozygous	109437534
1	170429757	170429758	C	T	35	GENIC	homozygous	108958826
1	170429824	170429825	G	C	46	GENIC	homozygous	108958827
1	170430150	170430151	A	G	43	GENIC	homozygous	108958828
1	170431046	170431047	A	G	53	GENIC	homozygous	108958829