chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	66737979	66737980	T	C	32	GENIC	homozygous	115888132
11	66738659	66738660	G	A	32	GENIC	homozygous	115888134
11	66738820	66738821	A	G	44	GENIC	homozygous	115888136
11	66743162	66743163	G	T	40	GENIC	homozygous	115888138
11	66743252	66743253	C	T	52	GENIC	homozygous	115888140
11	66743282	66743283	G	A	44	GENIC	homozygous	115888142
11	66743303	66743304	T	C	46	GENIC	homozygous	115888144
11	66744666	66744667	C	G	38	GENIC	homozygous	115888146
11	66744999	66745000	C	T	39	GENIC	homozygous	115888148
11	66747706	66747707	G	A	39	GENIC	homozygous	115888150
11	66748728	66748729	C	T	33	GENIC	homozygous	115888152
11	66752422	66752423	C	T	37	GENIC	homozygous	115888154
11	66752794	66752795	T	C	61	GENIC	homozygous	115888156
11	66753383	66753384	G	A	33	GENIC	homozygous	115888160
11	66753840	66753841	G	T	46	GENIC	homozygous	115888162
11	66753973	66753974	C	T	36	GENIC	homozygous	115888164
11	66755256	66755257	G	A	57	GENIC	homozygous	115888166
11	66755290	66755291	A	G	49	GENIC	homozygous	115888168
11	66756091	66756092	T	A	47	GENIC	homozygous	115888170
11	66756770	66756771	A	G	55	GENIC	homozygous	115888172
11	66757512	66757513	A	T	38	GENIC	possibly homozygous	115888174
11	66757542	66757543	T	C	41	GENIC	homozygous	115888176
11	66757719	66757720	A	T	56	GENIC	homozygous	115888178
11	66758118	66758119	A	T	26	GENIC	homozygous	115888180
11	66758278	66758279	T	C	35	GENIC	homozygous	115888182