chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108415653	108415654	G	A	26	GENIC	homozygous	117136432
10	108415960	108415961	C	A	24	GENIC	homozygous	117136433
10	108415961	108415962	T	C	24	GENIC	homozygous	117145223
10	108416077	108416078	G	A	28	GENIC	homozygous	117136434
10	108416402	108416403	G	A	34	GENIC	homozygous	117136435
10	108416505	108416506	A	G	36	GENIC	homozygous	116908793
10	108418313	108418314	C	G	34	GENIC	homozygous	117145225
10	108416220	108416221	T	C	28	GENIC	homozygous	116715850
10	108417681	108417682	T	A	37	GENIC	homozygous	116715852
10	108418170	108418170		ACACAGGACGGGCC	28	GENIC	homozygous	134229250
10	108418849	108418850	A	G	27	GENIC	homozygous	116715858
10	108418900	108418901	T	C	31	GENIC	homozygous	116715861
10	108419303	108419304	T	C	27	GENIC	homozygous	116908800
10	108420294	108420295	G	C	29	GENIC	homozygous	116715863
10	108420753	108420754	A	G	23	GENIC	homozygous	116908805
10	108420813	108420814	G	A	25	GENIC	homozygous	117136436
10	108420888	108420898	GCCAAGTACC		26	GENIC	homozygous	134229251
10	108421113	108421114	G	A	25	GENIC	homozygous	117136437
10	108421143	108421144	T	C	22	GENIC	homozygous	116908808
10	108421148	108421149	G	A	23	GENIC	homozygous	117136438
10	108422041	108422042	A	G	37	GENIC	homozygous	116715867
10	108423089	108423090	A	T	22	GENIC	homozygous	117136439
10	108423293	108423294	A	G	26	GENIC	homozygous	116908809
10	108423371	108423372	A	G	27	GENIC	homozygous	116908810
10	108423745	108423746	A	C	31	GENIC	homozygous	116715869
10	108424434	108424435	C	A	35	GENIC	homozygous	117136440
10	108424489	108424489		CTTTAAAACATGACGAGGGGTTTCTTT	26	GENIC	homozygous	134229252
10	108424629	108424630	A	T	19	GENIC	homozygous	116908811
10	108424868	108424869	A	C	15	GENIC	homozygous	116908812
10	108420138	108420139	C	T	33	GENIC	homozygous	116961750
10	108420145	108420146	A	G	34	GENIC	homozygous	116961752
10	108420147	108420148	C	T	34	GENIC	homozygous	116961754
10	108424941	108424942	C	T	14	GENIC	homozygous	117136441