chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	237894009	237894010	T	G	27	GENIC	homozygous	108577814
1	237894118	237894119	T	G	28	GENIC	homozygous	120818013
1	237894374	237894375	G	T	13	GENIC	homozygous	120818014
1	237894766	237894767	C	T	16	GENIC	homozygous	120818015
1	237894955	237894956	T	A	17	GENIC	homozygous	120818016
1	237894988	237894989	G	A	16	GENIC	homozygous	120818017
1	237895074	237895075	C	T	21	GENIC	homozygous	120818018
1	237895208	237895209	G	A	30	GENIC	homozygous	120818019
1	237895475	237895476	G	C	22	GENIC	homozygous	120818020
1	237896145	237896146	C	T	32	GENIC	homozygous	120818021
1	237897309	237897310	C	T	21	GENIC	possibly homozygous	120818022
1	237898457	237898458	A	T	18	GENIC	homozygous	108577828
1	237898599	237898600	C	G	21	GENIC	homozygous	108577830
1	237899581	237899582	A	G	32	GENIC	homozygous	108577836
1	237900295	237900296	C	G	24	GENIC	possibly homozygous	120818023
1	237900449	237900450	T	A	22	GENIC	possibly homozygous	120818024
1	237901581	237901582	A	G	24	GENIC	homozygous	108577842
1	237902290	237902291	A	G	29	GENIC	homozygous	108577844
1	237902516	237902517	T	C	28	GENIC	homozygous	108577846
1	237902620	237902621	T	C	31	GENIC	homozygous	108577848
1	237902874	237902875	G	A	41	GENIC	homozygous	120818025
1	237903019	237903020	C	T	41	GENIC	homozygous	120818026
1	237903198	237903199	G	A	45	GENIC	homozygous	120818027
1	237904394	237904395	C	T	37	GENIC	homozygous	120818028
1	237904539	237904540	C	A	29	GENIC	homozygous	108577856
1	237904984	237904985	A	G	37	GENIC	homozygous	108577858
1	237905194	237905195	G	T	28	GENIC	homozygous	120818029
1	237905959	237905960	A	C	37	GENIC	homozygous	120818030
1	237906169	237906170	C	G	39	GENIC	homozygous	120818031
1	237906627	237906628	G	A	18	GENIC	homozygous	108577868
1	237907454	237907455	A	G	29	GENIC	homozygous	108577872
1	237909864	237909865	C	A	31	GENIC	homozygous	108577882