chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	176171582	176171583	A	G	35	GENIC	homozygous	112218626
3	176175114	176175115	T	C	39	GENIC	homozygous	112218627
3	176176944	176176945	T	C	71	GENIC	homozygous	112218628
3	176176995	176176996	A	G	71	GENIC	homozygous	112218629
3	176177011	176177012	A	G	69	GENIC	homozygous	112218630
3	176178800	176178801	T	G	30	GENIC	homozygous	112218631
3	176186233	176186234	T	C	47	GENIC	homozygous	112218632
3	176189640	176189641	T	C	49	GENIC	homozygous	112218633
3	176189728	176189729	A	G	28	GENIC	homozygous	112218634
3	176190306	176190307	C	T	22	GENIC	homozygous	112218635
3	176192429	176192430	A	T	27	GENIC	homozygous	112218637
3	176192627	176192628	A	G	41	GENIC	homozygous	112218638
3	176194362	176194363	A	G	44	GENIC	homozygous	112218639
3	176196768	176196769	C	A	39	GENIC	possibly homozygous	112218640
3	176198083	176198084	G	T	14	GENIC	homozygous	112218641
3	176198620	176198621	C	T	28	GENIC	homozygous	112218642
3	176199805	176199806	A	G	19	GENIC	homozygous	112218643
3	176200257	176200258	T	C	49	GENIC	homozygous	112218644
3	176202217	176202218	A	G	47	GENIC	homozygous	112218645
3	176209611	176209612	T	G	38	GENIC	homozygous	112218648
3	176211639	176211640	G	A	37	GENIC	homozygous	112218649
3	176212209	176212210	G	A	26	GENIC	homozygous	112047833
3	176212360	176212361	C	G	8	GENIC	homozygous	112319237
3	176216246	176216247	A	T	42	GENIC	homozygous	112218650