chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	18081048	18081049	G	GT	43	GENIC	homozygous	51335556
10	18081101	18081105	TTTT	----	15	GENIC	possibly homozygous	51335557
10	18081457	18081458	T	C	47	GENIC	possibly homozygous	51335558
10	18081938	18081939	C	T	56	GENIC	homozygous	51628938
10	18083089	18083090	G	A	73	GENIC	possibly homozygous	51628939
10	18083677	18083678	G	A	61	GENIC	possibly homozygous	51335561
10	18084732	18084733	C	A	34	GENIC	heterozygous	51335563
10	18084919	18084920	C	CACAG	36	GENIC	homozygous	51335564
10	18085800	18085801	G	A	33	GENIC	possibly homozygous	51335565
10	18085828	18085829	T	C	31	GENIC	possibly homozygous	51335566
10	18085890	18085891	T	C	45	GENIC	possibly homozygous	51335567
10	18086676	18086677	T	A	68	GENIC	possibly homozygous	51335569
10	18086682	18086683	T	TTGAC	67	GENIC	homozygous	51335570
10	18087263	18087267	TTTT	----	1	GENIC	homozygous	51335571
10	18088224	18088225	A	C	53	GENIC	homozygous	51335572
10	18090720	18090721	G	T	46	GENIC	homozygous	51335574
10	18090780	18090781	A	G	48	GENIC	homozygous	51335575
10	18090853	18090854	A	G	61	GENIC	homozygous	51628940