chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	85387538	85387539	C	T	21	GENIC	homozygous	109504639
1	85389626	85389627	A	G	26	GENIC	homozygous	109504640
1	85390190	85390191	C	G	10	GENIC	homozygous	109504641
1	85390283	85390284	G	C	11	GENIC	homozygous	109504642
1	85391045	85391046	C	T	31	GENIC	homozygous	109504644
1	85391259	85391260	G	T	10	GENIC	homozygous	109504645
1	85391531	85391532	A	G	17	GENIC	homozygous	109504646
1	85391633	85391634	T	G	27	GENIC	homozygous	109504647
1	85392373	85392374	A	G	38	GENIC	homozygous	108882033
1	85392699	85392700	T	C	26	GENIC	homozygous	109504648
1	85392726	85392727	G	A	31	GENIC	homozygous	109504649
1	85393195	85393196	A	T	27	GENIC	homozygous	108882034
1	85393238	85393239	T	A	25	GENIC	homozygous	109504650
1	85393290	85393291	G	A	17	GENIC	homozygous	108882035
1	85394026	85394027	G	C	25	GENIC	homozygous	109504652
1	85394421	85394422	G	A	29	GENIC	homozygous	109504653
1	85394777	85394778	T	C	34	GENIC	homozygous	109504654
1	85396457	85396458	A	G	22	GENIC	homozygous	109504655
1	85396506	85396507	G	A	19	GENIC	homozygous	109504656
1	85398976	85398977	A	C	30	GENIC	homozygous	108882037