chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	111326567	111326568	G	A	13	GENIC	homozygous	111674351
3	111327197	111327198	C	T	18	GENIC	homozygous	112004930
3	111328103	111328104	G	A	18	GENIC	homozygous	111674353
3	111328465	111328466	G	A	20	GENIC	homozygous	111674355
3	111329213	111329214	G	A	19	GENIC	homozygous	111674356
3	111332060	111332061	C	T	19	GENIC	homozygous	111674359
3	111333679	111333680	A	T	12	GENIC	homozygous	112004934
3	111334201	111334202	A	T	16	GENIC	homozygous	111674362
3	111335931	111335932	A	G	10	GENIC	homozygous	111674364
3	111336817	111336818	G	A	29	GENIC	homozygous	111674366
3	111337044	111337045	T	C	27	GENIC	homozygous	111674367
3	111337201	111337202	A	G	22	GENIC	homozygous	111674369
3	111337577	111337578	C	A	11	GENIC	homozygous	111674371
3	111338561	111338562	G	A	17	GENIC	homozygous	111674373
3	111338618	111338619	T	C	22	GENIC	homozygous	111674375
3	111340796	111340797	A	T	25	GENIC	homozygous	111674377
3	111340808	111340809	T	C	27	GENIC	homozygous	111674379
3	111341442	111341443	T	C	22	GENIC	homozygous	111674381
3	111342284	111342285	T	C	29	GENIC	homozygous	112004938
3	111344870	111344871	T	C	27	GENIC	homozygous	111674386
3	111346731	111346732	T	C	21	GENIC	homozygous	111674392
3	111347747	111347748	G	A	24	GENIC	homozygous	112139179
3	111345621	111345622	C	T	21	GENIC	homozygous	112139178