chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9642765	9642766	C	G	17	GENIC	homozygous	111873597
3	9648380	9648380		AT	18	GENIC	homozygous	127848604
3	9649671	9649672	A	G	36	GENIC	homozygous	111443395
3	9652107	9652108	T	C	28	GENIC	homozygous	111443402
3	9652215	9652216	G	T	27	GENIC	homozygous	111443403
3	9653505	9653506	A	G	30	GENIC	homozygous	111873599
3	9653641	9653642	T	C	39	GENIC	homozygous	111443406
3	9654217	9654218	T	A	33	GENIC	homozygous	111873601
3	9654505	9654506	A	G	37	GENIC	homozygous	111443409
3	9654661	9654662	G	A	33	GENIC	homozygous	111873603
3	9656241	9656242	T	C	22	GENIC	homozygous	111443412
3	9654063	9654063		TGCTGC	30	GENIC	homozygous	130900423
3	9656957	9656958	A	G	22	GENIC	homozygous	111443413
3	9658362	9658363	T	C	27	GENIC	homozygous	111443414