chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	161299327	161299328	C	G	31	GENIC	homozygous	111797043
3	161299775	161299776	G	A	35	GENIC	homozygous	111797045
3	161299913	161299914	A	G	29	GENIC	homozygous	111797047
3	161300218	161300219	T	C	50	GENIC	homozygous	111797049
3	161300459	161300460	C	T	31	GENIC	homozygous	111797051
3	161300460	161300461	G	A	32	GENIC	homozygous	111797053
3	161301951	161301952	G	C	39	GENIC	homozygous	111797055
3	161302130	161302131	C	T	33	GENIC	homozygous	111797057
3	161302196	161302197	A	G	40	GENIC	homozygous	111797059
3	161302711	161302712	A	G	51	GENIC	homozygous	111797061
3	161302802	161302803	G	A	34	GENIC	homozygous	111797063
3	161302826	161302827	G	A	25	GENIC	homozygous	111797065
3	161302897	161302898	G	T	25	GENIC	homozygous	111797067
3	161303199	161303200	G	T	37	GENIC	homozygous	111797069
3	161303405	161303406	T	A	47	GENIC	homozygous	111797071
3	161303528	161303529	A	G	22	GENIC	homozygous	111797073
3	161303888	161303889	G	C	40	GENIC	homozygous	111797075
3	161303895	161303896	T	C	38	GENIC	homozygous	111797077
3	161303963	161303964	T	C	34	GENIC	homozygous	111797079
3	161303984	161303985	T	C	28	GENIC	homozygous	111797081
3	161304339	161304340	C	G	33	GENIC	homozygous	111797083
3	161304497	161304498	T	C	32	GENIC	homozygous	111797085