chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	176818083	176818084	T	C	22	GENIC	homozygous	112219167
3	176818523	176818524	A	G	20	GENIC	homozygous	112219168
3	176818960	176818961	G	T	32	GENIC	homozygous	112219169
3	176818983	176818984	A	T	32	GENIC	homozygous	111842700
3	176818990	176818991	G	A	35	GENIC	homozygous	112219170
3	176819021	176819022	G	A	38	GENIC	homozygous	112219171
3	176819451	176819452	A	G	19	GENIC	homozygous	111842702
3	176820519	176820520	G	A	29	GENIC	homozygous	112219173
3	176820780	176820781	T	A	31	GENIC	homozygous	111842704
3	176821056	176821057	T	A	25	GENIC	homozygous	112219174
3	176821648	176821649	C	G	10	GENIC	homozygous	112219176
3	176822673	176822674	T	A	22	GENIC	homozygous	112219177
3	176835016	176835017	G	T	28	GENIC	homozygous	111842720
3	176835809	176835810	A	G	22	GENIC	homozygous	111842722
3	176839291	176839292	G	A	15	GENIC	homozygous	111842726
3	176840392	176840393	A	C	26	GENIC	homozygous	111842728
3	176843752	176843753	G	A	30	GENIC	homozygous	111842730
3	176848120	176848121	C	T	25	GENIC	homozygous	112219179
3	176848333	176848334	A	C	32	GENIC	homozygous	112219180
3	176851082	176851083	G	T	25	GENIC	homozygous	112219181
3	176855491	176855492	A	G	22	GENIC	homozygous	111842750