chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	59996011	59996012	T	A	26	GENIC	homozygous	111584587
3	59998562	59998563	G	T	28	GENIC	homozygous	111584588
3	60000573	60000574	C	A	24	GENIC	homozygous	111584589
3	60001070	60001071	G	A	27	GENIC	possibly homozygous	111584590
3	60002268	60002269	C	T	35	GENIC	homozygous	111584591
3	60002453	60002454	A	G	11	GENIC	homozygous	111584592
3	60003051	60003052	C	T	19	GENIC	homozygous	111584593
3	60004875	60004876	C	T	25	GENIC	homozygous	111584594
3	60007332	60007333	C	T	43	GENIC	homozygous	111584595
3	60007526	60007527	C	A	41	GENIC	homozygous	111584596
3	60010066	60010067	C	G	29	GENIC	homozygous	111584597
3	60010680	60010681	G	C	25	GENIC	homozygous	111584598
3	60014184	60014185	T	A	49	GENIC	possibly homozygous	111584599
3	60014582	60014583	A	G	33	GENIC	homozygous	111584600
3	60016976	60016977	G	C	22	GENIC	homozygous	111584601
3	60017794	60017795	G	A	38	GENIC	homozygous	111584602
3	60017837	60017838	T	G	42	GENIC	heterozygous	112341125
3	60018646	60018647	C	G	22	GENIC	homozygous	111584603
3	60018668	60018669	A	G	24	GENIC	homozygous	111584604
3	60019120	60019121	A	G	23	GENIC	homozygous	111584605
3	60019186	60019187	G	A	30	GENIC	homozygous	111584606
3	60019490	60019491	A	G	25	GENIC	homozygous	111584607
3	60019528	60019529	C	T	30	GENIC	homozygous	111584608
3	60019667	60019668	G	A	30	GENIC	homozygous	111584609
3	60019726	60019727	C	T	29	GENIC	homozygous	111584610
3	60019743	60019744	C	T	31	GENIC	homozygous	111584611
3	60020100	60020101	A	G	29	GENIC	homozygous	111584612
3	60021436	60021437	C	T	40	GENIC	homozygous	111584613
3	60021545	60021546	G	T	35	GENIC	homozygous	111584614
3	60021878	60021879	A	G	32	GENIC	homozygous	111584615
3	60022106	60022107	G	A	41	GENIC	homozygous	111584616
3	60023532	60023533	G	A	29	GENIC	homozygous	111584624