chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	160019163	160019164	C	T	75	GENIC	homozygous	111791166
3	160019897	160019898	A	T	56	GENIC	homozygous	111791168
3	160020509	160020510	G	A	46	GENIC	homozygous	111791170
3	160021913	160021914	C	T	33	GENIC	homozygous	111791172
3	160021928	160021929	C	A	34	GENIC	homozygous	111791173
3	160023060	160023061	T	C	42	GENIC	possibly homozygous	111791175
3	160023427	160023428	T	C	33	GENIC	possibly homozygous	111791177
3	160025195	160025196	C	T	56	GENIC	homozygous	111791179
3	160027220	160027221	G	A	52	GENIC	homozygous	111791181
3	160028426	160028427	C	T	69	GENIC	homozygous	111791183
3	160029828	160029829	A	G	51	GENIC	homozygous	111791185
3	160030498	160030499	T	C	40	GENIC	homozygous	111791187
3	160033762	160033763	T	C	63	GENIC	homozygous	111791189
3	160035292	160035293	A	T	57	GENIC	homozygous	111791191
3	160035465	160035466	T	C	72	GENIC	possibly homozygous	111791193
3	160035634	160035635	G	A	62	GENIC	possibly homozygous	111791195
3	160036519	160036520	A	G	71	GENIC	homozygous	111791197
3	160036697	160036698	T	C	55	GENIC	homozygous	111791199
3	160036713	160036714	G	A	48	GENIC	possibly homozygous	111791201
3	160037672	160037673	G	A	46	GENIC	homozygous	111791203
3	160037953	160037954	A	G	49	GENIC	homozygous	111791204