chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	163768345	163768346	A	T	20	GENIC	homozygous	111805158
3	163769767	163769768	C	T	17	GENIC	homozygous	111805160
3	163771389	163771390	C	T	29	GENIC	homozygous	111805162
3	163774358	163774359	T	C	29	GENIC	homozygous	111805163
3	163774378	163774379	C	T	27	GENIC	homozygous	111805165
3	163774482	163774483	A	G	25	GENIC	homozygous	111805167
3	163775545	163775546	A	C	26	GENIC	homozygous	111805169
3	163775876	163775877	G	A	19	GENIC	homozygous	111805171
3	163776180	163776181	T	C	22	GENIC	homozygous	111805173
3	163777162	163777163	T	G	22	GENIC	homozygous	111805175
3	163778959	163778960	C	T	10	GENIC	homozygous	111805177
3	163779108	163779109	C	T	19	GENIC	homozygous	111805179
3	163780186	163780187	A	C	26	GENIC	homozygous	111805181
3	163781607	163781608	C	T	26	GENIC	homozygous	111805183
3	163781996	163781997	G	C	23	GENIC	homozygous	111805185
3	163782133	163782134	A	T	28	GENIC	homozygous	111805187
3	163783070	163783071	T	C	29	GENIC	homozygous	111805189
3	163783458	163783459	T	C	20	GENIC	homozygous	111805191
3	163783806	163783807	A	G	26	GENIC	homozygous	111805193
3	163783914	163783915	A	G	19	GENIC	homozygous	111805195
3	163784452	163784453	C	G	25	GENIC	homozygous	111805197
3	163785597	163785598	C	T	18	GENIC	homozygous	111805199