chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	18081048	18081049	G	GT	11	GENIC	homozygous	51335556
10	18081101	18081105	TTTT	----	7	GENIC	possibly homozygous	51335557
10	18081457	18081458	T	C	20	GENIC	homozygous	51335558
10	18082095	18082096	C	T	21	GENIC	homozygous	51335559
10	18082307	18082308	G	T	20	GENIC	homozygous	51335560
10	18083677	18083678	G	A	18	GENIC	homozygous	51335561
10	18083713	18083714	C	T	14	GENIC	homozygous	51335562
10	18084919	18084920	C	CACAG	28	GENIC	homozygous	51335564
10	18085800	18085801	G	A	9	GENIC	homozygous	51335565
10	18085828	18085829	T	C	10	GENIC	homozygous	51335566
10	18085890	18085891	T	C	16	GENIC	homozygous	51335567
10	18086676	18086677	T	A	22	GENIC	homozygous	51335569
10	18086682	18086683	T	TTGAC	22	GENIC	homozygous	51335570
10	18087263	18087267	TTTT	----	2	GENIC	homozygous	51335571
10	18088224	18088225	A	C	19	GENIC	homozygous	51335572
10	18090720	18090721	G	T	23	GENIC	homozygous	51335574
10	18090780	18090781	A	G	27	GENIC	homozygous	51335575
10	18084726	18084727	T	TCTCACACAAAAGCAAGGGTGCCACCA	37	GENIC	homozygous	52358082
10	18085608	18085616	TCTCTCTT	--------	6	GENIC	heterozygous	52358084
10	18090259	18090260	G	GTTTTTTTTTTTTTTTTGTCTAAAATATTTTTTTTTTATTAACTTGAGTATTTC	3	GENIC	heterozygous	52358088
10	18085610	18085616	TCTCTT	------	5	GENIC	heterozygous	53131909
10	18085927	18085928	T	TCC	13	GENIC	homozygous	53184951