chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	161930835	161930836	T	C	67	GENIC	homozygous	141561962
3	161931278	161931279	G	T	53	GENIC	possibly homozygous	144654151
3	161932043	161932044	C	T	63	GENIC	homozygous	141561963
3	161932281	161932287	TCCAGG		44	GENIC	homozygous	141486058
3	161932678	161932679	T	C	42	GENIC	homozygous	141561964
3	161932865	161932866	G	A	48	GENIC	homozygous	141561965
3	161933617	161933618	T	G	41	GENIC	homozygous	141561966
3	161934401	161934402	G	A	37	GENIC	homozygous	141561967
3	161934806	161934809	AAG		43	GENIC	homozygous	141486059
3	161934954	161934955	T	C	39	GENIC	homozygous	141561968
3	161935631	161935632	G	A	53	GENIC	homozygous	141561969
3	161935941	161935941		GC	44	GENIC	possibly homozygous	141486060