chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	18081048	18081049	G	GT	35	GENIC	homozygous	51335556
10	18081101	18081105	TTTT	----	18	GENIC	possibly homozygous	51335557
10	18081457	18081458	T	C	47	GENIC	possibly homozygous	51335558
10	18082095	18082096	C	T	27	GENIC	possibly homozygous	51335559
10	18082307	18082308	G	T	28	GENIC	homozygous	51335560
10	18083677	18083678	G	A	23	GENIC	homozygous	51335561
10	18083713	18083714	C	T	21	GENIC	homozygous	51335562
10	18084732	18084733	C	A	41	GENIC	heterozygous	51335563
10	18084919	18084920	C	CACAG	31	GENIC	homozygous	51335564
10	18085800	18085801	G	A	35	GENIC	possibly homozygous	51335565
10	18085828	18085829	T	C	32	GENIC	homozygous	51335566
10	18085890	18085891	T	C	33	GENIC	homozygous	51335567
10	18085927	18085928	T	TC	37	GENIC	homozygous	51335568
10	18086676	18086677	T	A	39	GENIC	homozygous	51335569
10	18086682	18086683	T	TTGAC	40	GENIC	homozygous	51335570
10	18087263	18087267	TTTT	----	1	GENIC	homozygous	51335571
10	18088224	18088225	A	C	23	GENIC	homozygous	51335572
10	18090137	18090138	C	A	24	GENIC	possibly homozygous	51335573
10	18090720	18090721	G	T	29	GENIC	homozygous	51335574
10	18090780	18090781	A	G	39	GENIC	homozygous	51335575