chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59344182	59344183	T	C	67	GENIC	homozygous	116511652
8	59344375	59344376	A	G	63	GENIC	homozygous	116511654
8	59344677	59344678	G	A	48	GENIC	possibly homozygous	116511658
8	59344722	59344723	G		38	GENIC	possibly homozygous	128595567
8	59345081	59345082	C	T	60	GENIC	homozygous	116511660
8	59345102	59345103	C	A	59	GENIC	homozygous	116511662
8	59345147	59345148	T	G	58	GENIC	homozygous	116511664
8	59345225	59345225		CGCTGCTGCCTCCTGTTCTG	59	GENIC	homozygous	128595568
8	59345232	59345233	A	G	60	GENIC	homozygous	116511666
8	59345336	59345337	T	C	66	GENIC	homozygous	116511668
8	59345566	59345572	GAGGGA		47	GENIC	homozygous	128595569
8	59345609	59345610	G	A	51	GENIC	homozygous	116511670
8	59345616	59345617	C	T	49	GENIC	possibly homozygous	116511672
8	59345651	59345652	T	C	56	GENIC	homozygous	116511674
8	59345743	59345744	T	A	59	GENIC	homozygous	116511676
8	59345852	59345853	A	G	62	GENIC	homozygous	116511678
8	59346110	59346111	A		52	GENIC	homozygous	128595570
8	59348071	59348072	A	T	38	GENIC	homozygous	116511680
8	59348203	59348204	T	G	12	GENIC	homozygous	117910606
8	59348271	59348272	A	G	25	GENIC	homozygous	116511682
8	59348482	59348483	T	G	48	GENIC	homozygous	116511684
8	59348534	59348534		C	40	GENIC	homozygous	128595571
8	59348757	59348758	T	C	48	GENIC	homozygous	116511688
8	59348950	59348951	G	A	56	GENIC	homozygous	116511690
8	59349311	59349312	C	A	48	GENIC	homozygous	116511692
8	59350150	59350151	C	T	49	GENIC	homozygous	116511694
8	59351030	59351031	G	A	37	GENIC	homozygous	116511696
8	59351126	59351127	C	T	52	GENIC	homozygous	116511698
8	59351438	59351439	A	G	59	GENIC	homozygous	116511700