chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9792829	9792830	A	G	53	GENIC	homozygous	111443612
3	9792877	9792878	C	T	50	GENIC	homozygous	119770315
3	9793247	9793248	C	T	61	GENIC	homozygous	111443614
3	9793303	9793304	T	G	67	GENIC	homozygous	111443615
3	9794262	9794263	G	A	55	GENIC	homozygous	111443617
3	9794443	9794444	A	G	64	GENIC	homozygous	111443618
3	9794460	9794461	C	T	64	GENIC	homozygous	111443619
3	9794746	9794747	T	C	47	GENIC	homozygous	111443620
3	9794756	9794757	T	C	47	GENIC	homozygous	111443621
3	9794883	9794884	A	C	54	GENIC	homozygous	119770317
3	9794903	9794904	T	C	59	GENIC	homozygous	111443622
3	9795064	9795065	C	T	52	GENIC	homozygous	111443623
3	9795292	9795293	G	T	46	GENIC	homozygous	119770319
3	9795377	9795378	T	C	50	GENIC	homozygous	111443625
3	9795479	9795480	C	T	58	GENIC	homozygous	111443627
3	9795489	9795490	C	G	60	GENIC	homozygous	111443628
3	9796242	9796243	T	C	59	GENIC	homozygous	119770321
3	9796272	9796273	T	C	56	GENIC	homozygous	111443630
3	9796296	9796297	A	T	55	GENIC	homozygous	111443631
3	9796562	9796563	T	G	67	GENIC	possibly homozygous	111443633
3	9796608	9796609	A	G	60	GENIC	homozygous	111443634
3	9796764	9796764		C	52	GENIC	homozygous	127848648
3	9797087	9797088	T	C	60	GENIC	homozygous	111443636
3	9797404	9797405	G	A	65	GENIC	homozygous	119770323
3	9797487	9797488	A	G	45	GENIC	homozygous	111443639
3	9798159	9798160	C	T	42	GENIC	homozygous	119770325
3	9798348	9798349	A	C	66	GENIC	possibly homozygous	111443641
3	9798633	9798634	C	G	50	GENIC	homozygous	111443642
3	9798714	9798715	A	G	42	GENIC	homozygous	111443643