chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	29289840	29289841	C	G	32	GENIC	homozygous	116540033
10	29290452	29290453	T	C	61	GENIC	homozygous	116540035
10	29296144	29296145	C	G	23	GENIC	homozygous	117986110
10	29296402	29296403	C	A	49	GENIC	homozygous	117986111
10	29296468	29296469	G	C	31	GENIC	homozygous	117986112
10	29296504	29296505	A	G	37	GENIC	homozygous	117327839
10	29296633	29296634	G	C	52	GENIC	homozygous	117001353
10	29296636	29296637	A	G	51	GENIC	homozygous	116540037
10	29296719	29296720	T	G	56	GENIC	possibly homozygous	116540039
10	29300456	29300457	T	C	57	GENIC	homozygous	116540041
10	29304225	29304226	G	T	55	GENIC	homozygous	116540043
10	29316320	29316321	A	G	50	GENIC	homozygous	116540049
10	29316541	29316542	T	G	68	GENIC	homozygous	116540051
10	29328612	29328613	T	A	65	GENIC	possibly homozygous	116540053
10	29332764	29332765	T	A	48	GENIC	homozygous	116540057
10	29334886	29334887	G	C	60	GENIC	homozygous	116540059
10	29296661	29296662	T	G	48	GENIC	homozygous	118034212
10	29296784	29296785	G	T	32	GENIC	homozygous	116751139
10	29328978	29328979	C	A	65	GENIC	homozygous	116751141