chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	164345706	164345707	T	C	35	GENIC	homozygous	111807192
3	164345984	164345985	C	T	26	GENIC	homozygous	111807194
3	164346030	164346031	T	C	28	GENIC	homozygous	111807196
3	164346112	164346113	C	A	35	GENIC	homozygous	111807198
3	164346971	164346972	C	T	36	GENIC	homozygous	112045839
3	164346972	164346973	T	C	36	GENIC	homozygous	112045840
3	164347035	164347036	G	A	34	GENIC	homozygous	111807202
3	164349897	164349898	T	C	39	GENIC	possibly homozygous	111807204
3	164350702	164350703	T	C	26	GENIC	homozygous	111807210
3	164352484	164352485	G	A	29	GENIC	homozygous	111807212
3	164354256	164354257	A	G	26	GENIC	homozygous	111807214
3	164355678	164355679	G	A	37	GENIC	homozygous	111807216
3	164355734	164355735	G	C	44	GENIC	homozygous	111807218
3	164356156	164356157	T	G	33	GENIC	homozygous	111807220
3	164357167	164357168	C	T	28	GENIC	homozygous	111807222
3	164357534	164357535	G	A	33	GENIC	homozygous	111807226
3	164357861	164357862	T	C	29	GENIC	homozygous	111807228
3	164357978	164357979	A	G	31	GENIC	homozygous	111807230
3	164359175	164359176	T	C	43	GENIC	homozygous	111807234
3	164359720	164359721	G	A	35	GENIC	homozygous	111807236
3	164359822	164359823	G	A	39	GENIC	homozygous	111807238
3	164360087	164360088	T	C	39	GENIC	homozygous	111807240
3	164360717	164360718	T	C	41	GENIC	homozygous	111807242
3	164362554	164362555	T	C	32	GENIC	homozygous	111807244
3	164363028	164363029	T	C	36	GENIC	homozygous	111807246
3	164363060	164363061	T	A	25	GENIC	homozygous	111807248
3	164365027	164365028	A	T	43	GENIC	homozygous	111807256
3	164365124	164365125	G	A	33	GENIC	homozygous	111807258
3	164365582	164365583	T	C	29	GENIC	homozygous	111807260
3	164365804	164365805	T	C	27	GENIC	homozygous	111807262
3	164365970	164365971	C	A	29	GENIC	homozygous	111807264
3	164366384	164366385	C	A	19	GENIC	homozygous	111807266
3	164366408	164366409	T	A	21	GENIC	homozygous	111807268